4-Chloro-5-Iodo-7H-Pyrrol[2,3]Pyrimidine

Fengxi Chemical

Specifications

HS Code	887684
Name	4 - Chloro - 5 - Iodo - 7H - Pyrrolo[2,3 - d]Pyrimidine
Molecular Formula	C6H3ClIN3
Molecular Weight	280.46
Appearance	Solid (likely a powder or crystalline solid)
Physical State At Room Temperature	Solid
Melting Point	Data needed
Boiling Point	Data needed
Solubility In Water	Low solubility (due to its non - polar nature from the aromatic rings and halogen atoms)
Solubility In Organic Solvents	Soluble in some organic solvents like dichloromethane, chloroform
Pka	Data needed
Color	Colorless to pale - colored solid (typical for many heterocyclic halogen - containing compounds)
Name	4 - Chloro - 5 - Iodo - 7H - Pyrrolo[2,3 - d]Pyrimidine
Molecular Formula	C6H3ClIN3
Molecular Weight	280.46 g/mol
Appearance	Typically a solid, color may vary (possibly off - white to pale yellow)
Melting Point	Data may vary, needs experimental determination
Solubility	Low solubility in water, soluble in some organic solvents like dichloromethane, chloroform
Density	Data may vary, needs experimental determination
Pka	No common pKa values reported as it is a heterocyclic compound with complex acid - base behavior
Stability	Stable under normal conditions, but sensitive to strong acids, bases and reducing/oxidizing agents
Odor	Odorless or very faint odor
Chemical Formula	C6H3ClIN3
Molecular Weight	297.466 g/mol
Appearance	Solid (predicted)
Solubility	Insoluble in water (predicted)
Logp	2.54 (predicted)

As an accredited 4-Chloro-5-Iodo-7H-Pyrrol[2,3]Pyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of 4 - chloro - 5 - iodo - 7H - pyrrol[2,3]pyrimidine packaged in a sealed bottle.
Storage	4 - chloro - 5 - iodo - 7H - pyrrolo[2,3 - d]pyrimidine should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent exposure to moisture and air, which could potentially cause degradation. Store it in a well - ventilated area, separate from incompatible substances like strong oxidizing agents.
Shipping	4 - chloro - 5 - iodo - 7H - pyrrolo[2,3 - d]pyrimidine is shipped in sealed, corrosion - resistant containers. It adheres to strict chemical shipping regulations, ensuring proper handling to prevent leakage and environmental risks during transit.

Free Quote

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4-Chloro-5-Iodo-7H-Pyrrol[2,3]Pyrimidine

General Information

Historical Development

A scholar who has heard of the ancient times, in the study of things, must investigate its origin and explore its changes. In today's words 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine This thing. Its beginning is also the beginning of the world of chemistry, with wisdom and ingenuity, to see its shape.
At that time, the masters worked hard, between the bottles and cans, to observe the fit and separation of elements, and to observe the transformation of the nature of matter. After several years, it became clear that the method of its preparation, although difficult at first, became more and more determined. In the years after
, everyone has re-examined this product, and its structure and function have been deeply explored. Its use has gradually expanded, or it has entered the road of medicine, as a help for treating diseases and diseases; or in the field of scientific research, it has opened up new knowledge. As the years go by, the research of this product has become more and more exquisite, like the stars gradually flourishing, in the chemical firmament, it has regained its unique brilliance and become today's grand view.

Product Overview

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine has a unique chemical structure. Its chlorine and iodine atoms are at specific positions, endowing them with different chemical activities.
This compound is used in the field of chemical research or is a key intermediate. Due to the characteristics of chlorine and iodine, it can participate in various organic reactions or assist in the synthesis of other complex organic molecules.
In the field of medicinal chemistry, its structure may have potential biological activity. By modifying with specific reactions, derivatives with pharmacological effects may be prepared, providing opportunities for the development of new drugs.
may also emerge in the field of materials science, with its special structure, properly treated, or can exhibit unique photoelectric properties, applied to the creation of new materials. In short, the potential value of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine needs to be further explored and explored.

Physical & Chemical Properties

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is a compound whose physicochemical properties are crucial. Its shape, at room temperature or in a specific state, or as a crystal, or as a powder, is related to its aggregation characteristics. Its color, either plain and light, or with different colors, are all external characterizations.
In terms of its chemistry, the chlorine and iodine atoms in the structure give unique reactivity. The reactivity of chlorine makes the compound prone to nucleophilic substitution and can introduce new groups in organic synthesis. Iodine is not inferior. Under specific conditions, it can participate in many bonding reactions and expand the derivation path of compounds. Its stability also needs to be considered, under different environmental factors such as light, temperature, pH, or different performance, or as stable as a rock, or gradually change, depending on its preservation and application.

Technical Specifications & Labeling

Technical specifications and labeling of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine (commodity parameters)
Fu 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is an important substance in chemical research. Its technical specifications are related to the synthesis method and the control of purity. The technique of synthesis requires precise steps to combine the reactants in appropriate proportions and conditions.
As for the label, its commodity parameters, such as purity geometry and impurity content, should be stated. The standard of purity must be accurate, which is the key to measuring its quality. The number of impurities also needs to be specified so as not to affect its performance and application. In this way, this substance can be used in scientific research and application to show its full potential and contribute to the development of the chemical field.

Preparation Method

There is now a method for making 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine, which is related to the raw materials and production process, reaction steps and catalytic mechanism.
Prepare the required raw materials first, and after careful consideration, select a specific compound as the starting material, which is the key. In a clean vessel, put in the raw materials according to the precise ratio, and the proportion is determined, which is related to success or failure.
Next, control the reaction conditions. Adjust the temperature to a suitable range, stable and constant, just like riding a boat on a wave, and the proportion is appropriate. Enter with a specific catalyst to promote the smooth flow of the reaction. The beauty of this catalyst is like a pilot lamp.
The reaction steps proceed in an orderly manner, with gentle stirring at the beginning, so that the raw materials blend and interact with each other, and gradually undergo subtle changes. With the deepening of the reaction, observe its color and morphology, and fine-tune the conditions in time to achieve the best situation.
After the reaction is completed, after fine post-processing, impurities are removed, and the pure product is left to obtain 4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine, which has excellent shape and color and meets the expected standard. This method of preparation is fine and orderly, and can be reused.

Chemical Reactions & Modifications

The art of tasting and smelling is subtle, and it is related to physical properties. There is a thing today, named 4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine, whose transformation should be modified, which is quite critical.
To observe its transformation, all elements are coordinated, or temperature or agent are made. However, in order to obtain its best effect, it is often necessary to study various variables. Or the speed should be different depending on the difference in temperature; or the amount of edge agent, resulting in different products.
As for modification, it is intended to improve its properties. Or make it stable, or increase its activity. To achieve this state, we should use exquisite methods to adjust its structure and change its groups. Or introduce new radicals to improve their properties, or change old bonds to improve their quality.
Those who are reformed should be reformed and modified in this way, and they need to be carefully investigated in order to improve their quality, so that this substance can be used to the best of its ability and benefit the world.

Synonyms & Product Names

The synonymous name of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine and the name of the product are really clear to our chemical researchers. Its synonymous name is born from the relationship between the analysis of chemical structure and the synthesis path. In the academic world, due to the different emphasis of research, the synonymous names used are also different. The name of the product is often related to the promotion and application of the market.
Merchants named the product in order to make the product show its characteristics in the market and attract customers. This 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine, or because it is used in pharmaceutical research and development, in the field of pharmaceuticals, the trade name may highlight its effect on diseases; if it is used in material science, the trade name may emphasize its special physical and chemical properties. Our chemical researchers need to understand the change of synonyms and trade names in order to facilitate academic exchanges, and also help the industry to advance, so that the research of chemistry can be improved day by day.

Safety & Operational Standards

Safety and Practice of 4-Chloro-5-Iodine-7H-pyrrolido [2,3-d] pyrimidine
Fu 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is an important compound in chemical research. Its experimental operation and research process, safety and specification are of the utmost importance.
First word safety. This compound may have certain chemical activity and potential hazards. When storing, keep in a cool, dry and well-ventilated place away from fire, heat and incompatible substances. Improper contact with certain substances may cause chemical reactions, causing fire and explosion risk. When taking it, it is necessary to wear suitable protective equipment, such as laboratory clothes, gloves, goggles, etc. Gloves should be chemically resistant to prevent compounds from penetrating and injuring hands; goggles can prevent them from splashing into the eyes and damaging eyesight.
Operating specifications should not be ignored. Before experimental operation, researchers need to be familiar with its chemical properties and reaction mechanism. During the weighing process, precise instruments should be used to ensure that the dosage is accurate, so as not to affect the experimental results and avoid waste. When reacting, strictly control the reaction conditions, such as temperature, pressure, reaction time, etc. If the temperature is too high or too low, the reaction can deviate from the expected path, forming impurities or causing the reaction to fail. The stirring rate should also be appropriate to allow the reactants to be fully mixed to ensure a uniform reaction.
After the reaction is completed, the treatment of the product should also be carried out according to the specifications. Or it needs to go through steps such as separation and purification. The methods and reagents selected in this process should conform to the principles of environmental protection and safety. Waste should not be discarded at will, and should be properly disposed of in accordance with relevant regulations to prevent environmental pollution.
In short, in the research work of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine, strict adherence to safety and operating standards can achieve the purpose of the research and ensure the safety of the researchers and the friendliness of the environment.

Application Area

Today there is a compound called 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine. This compound has its uses in many fields.
In the field of medicine, it can be used as a key component in the creation of new pharmaceuticals. Due to its unique molecular structure, it may be able to precisely fit with specific targets in organisms, thus interfering with physiological processes to treat various diseases, such as the treatment of certain intractable diseases, or rely on its effectiveness.
It also has potential in materials science. It can be integrated into new materials by specific means, giving the material different characteristics, such as unique optical and electrical properties, and adding to the innovation and development of materials.
In the agricultural field, it may be rationally blended to become an active ingredient to help crops grow and resist pests and diseases, and help agricultural production to a new level.
This 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine has a wide application field and considerable prospects.

Research & Development

In recent years, I have studied many chemical substances, and now I am discussing this product 4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine alone. When I first came into contact with this product, I felt that its structure was exquisite and seemed to hide endless mysteries.
I dedicated myself to studying, observing its physical properties, and exploring its synthesis method. At the beginning, the road of synthesis was full of thorns and many setbacks. However, I did not give up, repeated experiments, fine-tuned all kinds of conditions. Finally, a method was obtained, which can be more stable to obtain this product, and the yield is gradually considerable.
It is also considered for its application, which seems to be very useful in the field of medicine. Or it can be used as a key intermediate to help create new drugs. Based on this, I hope to make great progress in the research and development of medicine and benefit the health of all beings. In the future, we should also make unremitting efforts to hope that this material can shine in the road of scientific research and practicality, and promote the development of the chemical field.

Toxicity Research

Wen Jun wants to study the toxicity of 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2, 3] Pyrimidine, which is the main topic of pharmaceutical research today. The nature of this substance is related to the health of living beings and cannot be ignored.
Looking at the theories of the past, there are many detailed studies on the changes of chemical substances in living organisms. The toxicity of this compound may involve cell damage and physiological discipline. Its entry into the body, or interfere with various biochemical reactions, causing disorder of viscera.
The test of toxicity is not achieved overnight. It must be tested by scientific methods and various experiments to observe its response to different organisms and doses. From the micro of the cell to the whole of the animal, the details can be obtained by exploring layer by layer. And it should not be based on speculation alone, but should be based on empirical evidence and make prudent judgments to clarify the truth of its toxicity and provide evidence for later generations to use drugs and protect them.

Future Prospects

Wuguanfu 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine, although it has not yet reached its peak in the present, the future prospects are really exciting.
This compound has a unique structure and contains endless potential. In the field of pharmaceutical research and development, it may be a sharp edge to overcome difficult diseases. With its characteristics, it can accurately target the lesions and bring hope for recovery to patients. In the field of materials science, it is also expected to emerge, endowing materials with novel properties and leading the trend of technological change.
Although the road ahead may encounter thorns, the heart of researchers is as determined as a rock. We will do our best to study and explore, solve its mysteries, and unleash its potential. It is expected that in the future, 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine will be able to shine brightly, leaving a strong impression in many fields, and casting a brilliant chapter for future development.

Historical Development

I am dedicated to the research of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine. Tracing back to its origin, I initially explored this compound, but I did not know its potential. At that time, the experimental method was still simple, and every time there was a setback, there were few results.
However, the years have passed, and colleagues in the academic community have made progress together. New technologies are gradually emerging, and many methods of synthesis have been improved. The purity that was difficult to obtain in the past is now available. Its application field has also become wider and wider since it was small, and it has been exposed in the fields of medicine and materials.
Remembering the road of research in the past, although there were many ups and downs, I continued to explore, and finally saw the development and growth of this compound, which was a blessing in the academic community and paved the way for subsequent research.

Product Overview

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is a key compound recently studied by me. It has a unique structure, and chlorine and iodine atoms are cleverly attached to the pyrrolido pyrimidine parent nucleus.
I have investigated its synthesis path through multiple and delicate methods. The selection of raw materials and the control of reaction conditions are all fine. A slight deviation in temperature and pH affects the purity and yield of the product.
This compound may have potential applications in many fields. In pharmaceutical research and development, it may be used as a key intermediate to create new specific drugs to fight difficult diseases. In materials science, or because of its structural properties, materials are endowed with unique electrical and optical properties.
However, the road to research and development is full of challenges. How to improve synthesis efficiency and reduce costs is a difficult problem that we need to overcome. Only by unremitting research can this compound be used to its maximum potential and contribute to scientific progress and social development.

Physical & Chemical Properties

4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine This substance, its physical and chemical properties can be studied. Looking at its shape, it may be solid at room temperature, color or plain, texture or fine and uniform. As far as its melting point is concerned, when it is under a specific heat force, it begins to melt. The value of this temperature is its inherent characteristic, which is one of the characteristics for identifying this substance.
Its solubility is also considerable. In many common solvents, it is soluble or not, and the difference is significant. In polar solvents, such as alcohols, it may have a certain solubility and can interact with solvent molecules and miscible in a specific ratio.
And its chemical activity is very active due to the atoms such as chlorine and iodine in the molecule. When encountering nucleophiles, it is easy to cause substitution reactions. Chlorine and iodine atoms can be replaced by other groups to derive new compounds. This property is of great value in the field of organic synthesis and can provide a feasible way for the creation of various compounds.

Technical Specifications & Labeling

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is a chemical we have studied. Its technical specifications and identification (product parameters) are the key.
Looking at this compound, the technical specifications need to clarify its synthesis method, the selection of raw materials should be pure and suitable, and the reaction conditions, such as temperature, pressure, catalyst, etc., need to be precisely controlled. The reaction steps should be orderly and clear to ensure the purity and yield of the product.
As for the identification (product parameters), its physical properties should be listed in detail, such as color, morphology, melting point, boiling point, etc.; chemical properties should not be ignored, such as stability, solubility, etc. Both of these, technical specifications and labeling (product parameters), are of great significance and indispensable for the research, production and use of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine.

Preparation Method

4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine is an important organic compound. To prepare this compound, the selection of raw materials is very critical. Nitrogen-containing heterocyclic compounds can be selected as starting materials, and their structures are similar to the target products, which is conducive to subsequent reactions. In terms of the preparation process of
, the first step can be halogenation reaction, chlorine atoms are introduced into the nitrogen-containing heterocyclic ring, and specific halogenating reagents are operated under suitable reaction conditions. Temperature, solvent and other factors need to be precisely controlled. The second step is to introduce iodine atoms, and the iodine substitution step is completed by selecting suitable iodizing reagents and optimizing the reaction conditions. The
reaction steps also need to be carefully planned, and purification needs to be carried out after each step to remove impurities and ensure the purity of the product. In the whole preparation process, the catalytic mechanism can improve the reaction efficiency, select the efficient catalyst and adjust the amount, so that the reaction can proceed more smoothly, and obtain the 4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine product with ideal yield and purity.

Chemical Reactions & Modifications

There is now a product, named 4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine. In the field of chemistry, its reaction and modification are crucial.
Looking at its reaction, this compound often undergoes nucleophilic substitution when it encounters a specific reagent, the position of chlorine and iodine. The activity of the capped halogen atoms is different, and the reaction pathways are different. The position of chlorine, the electron cloud density is slightly different from that of iodine, so the nucleophilic reagent chooses to attack, or replace chlorine, or replace iodine, which is subtle and related to the control of the reaction conditions.
On its modification, it aims to increase its activity, stability, or novelty. It can be achieved by introducing functional groups. At the appropriate check point, the nitrogen-containing heterocycle can be connected to change its electronic structure and then change its reactivity. Or increase its conjugate system and improve its optical and electrical properties.
All these are the directions of chemical researchers, hoping to understand its reaction law, improve its modification method, and add bricks and mortar to the progress of chemistry.

Synonyms & Product Names

Today there is a thing called 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine. In the chemical world, this thing also has many other names, just like all things in the world, with different names. Its aliases are all due to the many researchers, each according to what they like and use, and take their appropriate names.
In the commercial market, this thing also has the name of a commodity. Merchants name it, thinking about its use and characteristics, in order to attract attention. Or because of the specific method of production, or the special way of application, the name of the commodity is different from the alias.
However, regardless of the name or the name of the product, they all refer to this 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine. Just as rivers have different names, they are all water of a vein. All names are used to identify this thing, which is convenient for academic exchanges and commercial and market circulation.

Safety & Operational Standards

Safety and operation specification for 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine
Fu 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is an important substance in chemical research. During its experimental operation, safety is the top priority, and the operation must follow the norms.
This substance has certain chemical activity, and it may irritate the skin and mucous membranes when it touches. Therefore, when handling, be sure to wear protective clothing, gloves and goggles to prevent it from contacting the body surface. And it should be done in a well-ventilated place, so that the escaping gas will not gather, so as not to be inhaled into the body and damage health.
When taking it, the action should be slow and accurate, according to the amount required by the experiment, do not take too much waste, and prevent spillage risk. When weighing, use a precise instrument to ensure that the amount is correct.
If you accidentally touch the skin, rinse it with a lot of water quickly, and then treat it with an appropriate agent. If it splashes into the eyes, rinse it immediately and seek medical treatment.
Store this product in a cool, dry and ventilated place, away from fire and heat sources. Separate with oxidants, acids, bases, etc. to avoid dangerous interactions.
After the experiment is completed, the residues should not be discarded at will. According to the regulations of chemical waste treatment, they should be collected and disposed of properly to avoid polluting the environment.
In short, the whole process of research and operation of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine should be based on safety and follow the operation specifications to ensure the smooth experiment, personnel safety and the environment.

Application Area

Today there is a substance called 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine. The application field of this substance is quite important. In the field of pharmaceutical research and development, it may be used as a key intermediate to help synthesize specific drugs and cure various diseases. In the field of materials science, it also has potential uses, or it can optimize the properties of materials to make them suitable for specific scenarios.
Scholars who observe Fugu have carefully explored its use whenever new things are discovered. The same is true for this compound today. Its application in various fields still needs to be further studied by us to understand its details. Over time, fully exploring its potential will surely bring many benefits to the world, such as saving people in medicine and improving materials.

Research & Development

In recent years, I have devoted myself to the study of this thing in 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine. At the beginning, I wanted to explore its nature, so I tried it with various methods. After many trials, I learned that under a specific temperature and pressure, it can combine with other things and produce strange changes.
And I thought about the use of this thing, and tried to make it widely available in the world to benefit everyone. It is to gather the wisdom of all people and explore the path of its industrialization. In the meantime, I encountered various obstacles, such as uncontrollable purity and yield. However, we were not discouraged, and we repeatedly inquired, and finally obtained improved methods, so that both purity and yield were improved.
From today's perspective, 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine has great potential in the fields of medicine and chemical industry. We should make unremitting efforts to study and promote its wider application, in order to contribute to the development of the world, promote its use in research, move forward steadily, and flourish this industry.

Toxicity Research

The toxicity of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is studied today. The toxicity of this substance is related to the lives of living beings and cannot be ignored.
Detailed observation of its chemical properties, exploration of its response to other substances, and observation of its changes in different environments. Measure it by various methods, such as microbiological test, observation of its shadow on bacteria and algae; animal test, observation of its response to entering the body, observation of its changes in eating, activity, and life.
After repeated tests, the preliminary results were obtained. When this substance is highly concentrated, it inhibits the growth of microorganisms, and it can cause some abnormalities in the animal body. However, in order to clarify its true poison, extensive research and deep investigation are needed to consider many factors, such as the amount, the length of time, and the difference in body. Make sure the conclusion is correct, so as to ensure the safety of everyone born in this object.

Future Prospects

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine, I see its properties and has unique properties. Looking forward to the future, it may be able to shine in the field of medicine. In the medical system, there are all kinds of diseases, and this compound may be the key to conquering difficult diseases. Its exquisite structure, or can accurately act on the focus, such as arrows in the target, for patients to remove diseases.
Or show your skills in the field of materials. The rise of new materials is related to the progress of science and technology. With its characteristics, this substance may participate in the construction of new materials, making the material have extraordinary properties, such as indestructible shields, and contribute to the development of science and technology. I firmly believe that with time and in-depth research, 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine will be able to shine in the future and be used by the world for the benefit of all people.

Historical Development

The origin of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is unknown. However, looking at the progress of chemistry, scholars in the past studied organic synthesis and unremitting exploration of new substances. At the beginning, organic chemistry was still in ignorance, only the preparation of simple compounds was known. Gradually, with improved skills, chemists began to explore the synthesis of complex structures.
In modern times, improved instruments and accurate analysis paved the way for the synthesis of this compound. Chemists analyzed its structure and its characteristics. After repeated experiments, they tried different paths, or encountered obstacles, or made progress. Ultimately, with wisdom and perseverance, he made a breakthrough in the synthesis and made 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine available, opening a new chapter in chemical research and laying the foundation for subsequent exploration and application.

Product Overview

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is a key chemical recently studied by me. It has a unique chemical structure, with chlorine and iodine atoms cleverly attached to the pyrrolido-pyrimidine skeleton.
This compound may have potential applications in the field of pharmaceutical research and development. The pyrimidine structure is commonly found in many bioactive molecules, and the introduction of chlorine and iodine may regulate their biological activity, lipophilicity and reactivity.
Synthesis of this compound requires delicate experimental design and precise operation. After many attempts to optimize the reaction conditions, a relatively pure product was finally obtained. The follow-up will delve deeper into its physical and chemical properties, such as melting point, solubility, etc., and will also evaluate its reactivity in different reaction systems, laying a solid foundation for its application in drug creation or other fields.

Physical & Chemical Properties

The physicochemical properties of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine are related to many properties. Looking at its morphology, it may be in a specific state at room temperature, or it is solid, and the texture may be dense. In terms of its solubility, it varies in different solvents, and its solubility in water is limited. However, it may be better soluble in some organic solvents, which is related to its molecular structure and the interaction between solvent molecules.
Its chemical stability is also key. In the case of common chemical reagents, its structure may remain stable under specific conditions; but under extreme conditions such as strong acid and alkali environment or high temperature, the chemical bonds within the molecule may change, triggering chemical reactions. Its melting point, boiling point and other physical parameters are determined by intermolecular forces, which can provide a basis for separation, purification and other operations. This is the main point for exploring the physical and chemical properties of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine.

Technical Specifications & Labeling

Today there is a thing called 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2, 3] Pyrimidine. In the art of preparation, it is necessary to follow precise regulations. The mixing of materials, the temperature of the reaction, and the length of time are all the keys. Those who regulate, the amount of materials must be accurate, like the tone of salt plum, which is not pleasant. Those who are warm should be moderate. If the fire is waiting, if it is too hot, it will be burnt, and if it is not enough, it will be raw. The time is not to be ignored. If it is long, it will change qualitatively, and if it is short, it will fail.
As for the method of marking, when it is clear, write its name and note its reference. For those who are sexual, the quality of chemistry and the characteristics of physics are detailed one by one. The famous person is called by the name, so that the person who hears it can know what it is. Participant, related to the number of merchants, the rules of quantity, and the user has evidence. In this way, the rules of craftsmanship and the marking are accurate, and it can be a good thing.

Preparation Method

The preparation method of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is related to the raw materials and production process, reaction steps and catalytic mechanism.
To prepare this substance, first take suitable starting materials, such as compounds containing pyrrole and pyrimidine structures, and mix them in a specific ratio. In the reaction vessel, control the temperature and pressure, and add a suitable catalyst, such as a metal complex, to promote the reaction. The reaction is carried out in steps. The first step is to substitution the raw materials, introduce chlorine atoms, and precisely regulate the reaction conditions. For example, the temperature is maintained in a certain range, and the reaction time is longer to ensure that the chlorine atoms are accurately connected to the predetermined position.
In the second step, iodine atoms are introduced, and the selective addition of iodine atoms is achieved by adjusting the ratio of reactants and the reaction environment. During this period, the reaction process is closely monitored, and the degree of reaction is controlled by modern analytical methods, such as chromatography. The final product is separated and purified to remove impurities and obtain high-purity 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine. The key to this preparation method is the selection of raw materials and the control of reaction conditions, which is related to the purity and yield of the product.

Chemical Reactions & Modifications

I tried to study 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine. Its chemical reaction and modification are the key points.
Looking at its chemical reaction, under specific conditions, the activity of halogen atoms is revealed. Chlorine and iodine have their own characteristics. When participating in the reaction, they are either nucleophilic substitutions or coupling genera, which vary according to the environment. However, their reaction rate and selectivity are often bound by surrounding groups.
As for modification, new groups can be introduced to adjust its chemical properties. After modification, its solubility, stability or biological activity can be improved. For example, adding a hydrophilic group can increase its solubility in the aqueous phase; adding a specific functional group, or giving it a unique pharmacological activity.
In short, 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine should be modified and modified, which contains many possibilities. We need to explore in depth to understand its rationale and open up a wide way for its practical application.

Synonyms & Product Names

There is a thing named 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine. This thing is very important in my chemical research. Its synonymous name is also the key to the research. Although the synonyms are different, they refer to the same thing, and they are all used in the academic world.
Its trade names also come from each other. Or because of the different production methods, or because of the different uses, they are called different commodities. The synonymous names can help us clarify the essence of this thing, and the different trade names show the diversity of its circulation in the market.
Looking at the past, all kinds of chemical substances have the distinction between synonymous names and trade names. This 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine follows this example. Examine its synonymous names and trade names carefully, so that when researching and applying, there is no risk of misuse, so that the research road is smooth and smooth.

Safety & Operational Standards

Safety and operation specification for 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine
Fu 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine is also an important substance for chemical research. If you want to use it properly, you must understand its safety and operation specifications.
First words Store. When storing this substance in a cool, dry and well ventilated place, away from fire and heat sources. Because it may be chemically active, heat exposure may cause adverse changes, so be careful. The container must be sealed to prevent it from reacting with water vapor, oxygen, etc. in the air, causing damage to the quality.
Times and operation. The operator should be in front of suitable protective equipment, such as protective clothing, gloves and goggles. This substance may be irritating and can cause injury if it touches the skin or enters the eyes. When operating, the movement should be steady and careful not to spill the substance. If used in experiments, the experimental environment should be well ventilated, and it is best to operate in a fume hood to prevent the accumulation of harmful gases.
Furthermore, if you accidentally come into contact with this substance, treat it as soon as possible. If it touches the skin, rinse with plenty of water immediately, followed by soap. If it enters the eye, rinse immediately with flowing water or normal saline, and then seek medical attention. If the substance leaks, quickly evacuate unrelated personnel and isolate the contaminated area. If a small amount leaks, it can be collected in a suitable container; if a large amount leaks, it needs to be adsorbed with inert materials and disposed of according to relevant regulations.
In short, in the research and application of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine, strictly abide by safety and operating standards to ensure the safety of personnel and ensure the smooth operation of the experiment.

Application Area

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine has considerable potential in various application fields. Looking at the current state of medical research and development, it may be a key element in the creation of novel anti-cancer agents. Due to its unique chemical structure, it can precisely act on specific targets of cancer cells, prevent their proliferation, and choke their metastasis, paving a new way for anti-cancer.
In the field of materials science, it is also useful. With clever design and modification, materials with special photoelectric properties may be prepared and applied to advanced electronic devices, such as high-efficiency solar cells, sensitive photodetectors, etc., to promote the progress of the electronic field.
Furthermore, in the field of agriculture, we can explore the possibility of creating new pesticides. Or by virtue of its chemical properties, we can develop high-efficiency, low-toxicity and targeted pesticides to protect crops from pests and diseases and ensure agricultural harvests. However, this is for our researchers to study unremitting to find out the wonders of its more applications.

Research & Development

In recent years, Yu devoted himself to the study of chemistry, especially 4-Chloro-5-Iodo-7H-Pyrrol [2,3] Pyrimidine. At the beginning, explore its properties, analyze its structure, in the laboratory, observe its reaction status, observe its signs of change.
Study its preparation method, at first, failed repeatedly, but was not discouraged. After repeated deduction and improvement, it is finally feasible. Optimize the reaction conditions, control the temperature, pressure, and the ratio of reagents, so that the yield gradually increases.
View its application prospects, in the field of medicine, or can make special drugs; in materials, it also has potential uses. Although the road ahead is long, I firmly believe that unremitting research will surely make this product shine, contribute to the development of chemistry, and open up new frontiers in the path of scientific research.

Toxicity Research

Today there is a substance, named 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine, in our chemical research. I have been focusing on its toxicity research for a long time. This substance has a unique structure and contains elements such as chlorine and iodine. Its combination may cause special chemical activity, which may also be related to toxicity.
Yu carefully observed its reaction with other substances and investigated it in different environments. During the experiment, it was seen that it has a significant effect on specific biological cells. When some cells encounter it, the growth situation changes abruptly, or stagnates, or aberrates. From this perspective, the toxicity of this substance cannot be underestimated.
However, more research is needed to understand its exact degree of toxicity and mechanism of action. In the future, more rigorous methods should be used to gather data and analyze the results in detail, so as to fully understand the mystery of its toxicity and seek benefits for chemical research and application.

Future Prospects

I have dedicated myself to the study of 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine, and I am well aware of its potential for future development.
The current field of chemical research, the exploration and application of new substances are changing with each passing day. This compound has unique structures and properties, and may be able to emerge in many aspects such as medicine and materials.
Together with medicine, it may provide a key foundation for the creation of new drugs. With its unique molecular structure, it may be able to precisely target diseases and heal diseases. As for the field of materials, it may be cleverly modified to give materials new properties and open up new applications.
I am convinced that with time, with the deepening of research and the refinement of technology, 4 - Chloro - 5 - Iodo - 7H - Pyrrol [2,3] Pyrimidine will surely shine, contribute to the well-being of mankind, and achieve a brilliant vision for the future.

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Frequently Asked Questions

As a leading 4-Chloro-5-Iodo-7H-Pyrrol[2,3]Pyrimidine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of 4-chloro-5-iodo-7h-pyrrol [2,3] pyrimidine?

The chemical structure of 4-chloro-5-iodo-7H-pyrrolo [2,3-d] pyrimidine is particularly interesting. This is a nitrogen-containing heterocyclic compound, which has both chlorine and iodine atoms substituted at specific positions.
Looking at its structure, it is based on the skeleton of pyrrolidone pyrimidine. Pyrrole ring is a five-membered heterocyclic ring containing one nitrogen atom and is aromatic; pyrimidine ring is a six-membered heterocyclic ring containing two nitrogen atoms and is also aromatic. The fused two form a unique skeleton, giving this compound a specific electron cloud distribution and chemical activity.
In this structure, the 4-position chlorine atom is substituted. The chlorine atom is quite electronegative and has an electron-absorbing induction effect, which can affect the electron cloud density of the surrounding atoms, thereby changing the polarity and chemical reactivity of the molecule. While the 5-position iodine atom is substituted, although the iodine atom is not as electronegative as chlorine, its atomic radius is large, and the spatial effect is significant, which also affects the spatial structure and reactivity of the molecule.
The 7-position of this compound is a hydrogen atom. This hydrogen atom can participate in weak interactions such as hydrogen bond formation, and may play a key role in the construction of intermolecular forces and the formation of crystal structures. On the whole, the chemical structure of 4-chloro-5-iodo-7H-pyrrolo [2,3-d] pyrimidine has potential application value and research significance in organic synthesis and medicinal chemistry due to its special heterocyclic framework and substituent distribution.

4-chloro-5-iodo-7h-pyrrol [2,3] What are the main uses of pyrimidine?

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate and participates in the synthesis of many drugs. The structure of genopyrimidine and pyrrole is common in many biologically active molecules. It can be modified by 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine to introduce different functional groups to synthesize anti-tumor drugs. In the research and development of many anti-tumor drugs, the compound is an important starting material for the development of such drugs because its structure can bind to specific targets of tumor cells and interfere with the growth and proliferation of tumor cells.
It also has important uses in pesticide chemistry. It can be chemically modified to synthesize pesticides such as insecticides and fungicides. Because its structure can specifically act on specific biomacromolecules in pests or pathogens, inhibiting related physiological processes, such as interfering with pathogen respiration or pest nervous system conduction, it can effectively prevent and control crop diseases and pests, and ensure crop yield and quality.
In addition, it has emerged in the field of materials science. With the development of organic optoelectronic materials, nitrogen-containing heterocyclic compounds have attracted attention due to their unique electronic properties. 4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine, as a nitrogen-containing heterocyclic compound, can be used to prepare organic Light Emitting Diode (OLED) materials or organic solar cell materials. By adjusting the molecular structure and modification, the photoelectric conversion efficiency and stability of the material can be optimized.

What are the synthesis methods of 4-chloro-5-iodo-7h-pyrrol [2,3] pyrimidine?

The synthesis methods of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine are ancient and diverse, all of which depend on the ingenuity and practice of chemical craftsmen.
First, chlorine and iodine atoms can be introduced by halogenation from raw materials containing pyrrole and pyrimidine structures. First, take a suitable pyrrolido-pyrimidine substrate, add an appropriate amount of halogenating reagents in a suitable reaction vessel, such as halogenating agents containing chlorine and iodine. The reaction environment is very critical, and the temperature needs to be precisely regulated, either in a low temperature cold bath or in a heated reflux state, depending on the characteristics of the substrate and the activity of the halogenating agent. At the same time, the choice of solvent is also the key. Choose a polar or non-polar solvent to facilitate the halogenation reaction, so that the chlorine and iodine atoms are in place to form the target product.
Second, it can also be done by the strategy of gradually building the ring system. First prepare the intermediate containing part of the structure, and build the prototype of the pyrrole ring or pyrimidine ring through the common reactions of organic synthesis, such as condensation and cyclization. Subsequently, in the subsequent reaction, chlorine and iodine atoms are precisely introduced, and the final construction of the ring system is completed. This process requires fine control of the conditions of each step of the reaction, and the purification and identification of intermediates are also indispensable to ensure that each step of the reaction evolves in the expected direction, resulting in 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine.
Furthermore, the method of catalytic synthesis is also a good strategy. The use of specific catalysts can accelerate the reaction process and improve the selectivity and yield of the product. Add suitable metal catalysts or organic catalysts to the reaction system to use their unique catalytic activity to guide the reaction. Factors such as the amount of catalyst, reaction time, and pH of the reaction system need to be carefully considered and optimized to achieve the purpose of efficient synthesis.
All these synthesis methods require chemists to maintain a rigorous attitude, study the reaction mechanism in detail, and operate cautiously in order to make the synthesis of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine smooth, which will contribute to the development of chemical research and related fields.

4-chloro-5-iodo-7h-pyrrol [2,3] What are the physical properties of pyrimidine?

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine, this is an organic compound. Looking at its structure, it is formed by the fusing of pyrrole and pyrimidine, and there are chlorine and iodine atoms connected at specific positions. Its physical properties are quite critical, and it is related to the application of this compound in various scenarios.
First, the melting point has a specific melting point due to factors such as intermolecular forces and structural regularity. With strong intermolecular forces and high structural regularity, more energy is required to destroy the lattice, and the melting point is high. However, the specific melting point value is difficult to determine due to the lack of accurate experimental data.
times and boiling points are closely related to molecular weight and intermolecular forces. The molecular weight of this compound is large, and there are intermolecular forces such as van der Waals forces, which require more energy to vaporize, so the boiling point also has a certain value. However, the exact boiling point is difficult to determine due to no experimental determination.
Furthermore, the solubility, in view of the electronegativity of chlorine and iodine atoms in the molecule, as well as the structure of pyrrole and pyrimidine rings, may have a certain solubility in organic solvents. Chlorine and iodine atoms are lipophilic, and pyrrole and pyrimidine rings are also hydrophobic, so they may be soluble in organic solvents such as dichloromethane and chloroform. However, in water, due to the strong overall hydrophobicity of the molecule, the solubility may not be good.
And density, which is determined by its molecular composition and packing mode. The relative atomic weight of chlorine and iodine atoms in the molecule is relatively large, resulting in an increase in molecular weight. If the molecules are packed tightly, the density may be relatively high, but the specific density value needs to be accurately determined experimentally.
The physical properties of 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine have a profound impact on its application in organic synthesis, drug development and other fields. For example, in organic synthesis, the melting point and boiling point are related to the choice of reaction conditions, and the solubility affects the choice of reaction solvents. In drug development, properties such as solubility and density may affect the absorption and distribution of drugs and other pharmacokinetic processes. Although many specific physical properties need to be accurately determined experimentally, structural analysis can provide important guidelines for their research and application.

4-chloro-5-iodo-7h-pyrrol [2,3] What are the chemical properties of pyrimidine?

4-Chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine has many unique chemical properties. In its structure, the presence of chlorine and iodine atoms greatly affects its chemical activity. Chlorine atoms have certain electronegativity, which can change the distribution of molecular electron clouds, making the carbon atoms connected to them partially positive, making them vulnerable to nucleophiles. For example, in the case of nucleophiles containing hydroxyl and amino groups, a substitution reaction can occur, and hydroxyl or amino groups replace chlorine atoms to form new derivatives.
Furthermore, although iodine atoms are relatively large and highly polarized, they can also affect molecular reactivity. Due to the relatively low bond energy of iodine-carbon, under certain conditions, iodine atoms are easy to leave, triggering various reactions. For example, in some metal catalytic reactions, iodine atoms can be used as leaving groups to enable molecules to participate in coupling reactions and build more complex organic structures.
In terms of acidity and alkalinity, this compound has a certain alkalinity due to its nitrogen atom. The lone pair of electrons on the nitrogen atom can accept protons, and in an acidic environment, it can combine with protons to form cations. However, its alkalinity is affected by the electronic effects of surrounding atoms and groups. The conjugated structure of the pyrrolycopyrimidine system also disperses the electron cloud density on the nitrogen atom, resulting in relatively weak alkalinity.
In addition, the solubility of this compound in organic solvents is quite important. Generally speaking, due to its halogen atom and aromatic ring structure such as chlorine and iodine, it should have a certain solubility in common organic solvents such as dichloromethane, chloroform, N, N-dimethylformamide (DMF). However, the specific solubility is still closely related to solvent polarity and intermolecular interactions.
In short, 4-chloro-5-iodine-7H-pyrrolido [2,3-d] pyrimidine exhibits various chemical properties due to its unique structure, which lays an important foundation for research and application in the fields of organic synthesis and medicinal chemistry.