4-Chloro-5-Iodo-7-(2-C-Methyl-Beta-D-Ribofuranosyl)-7H-Pyrrolo[2,3-D]Pyrimidine

Fengxi Chemical

Specifications

HS Code	328561
Chemical Formula	C11H14ClIN4O4
Molecular Weight	432.61
Appearance	Solid (predicted)
Melting Point	No data available
Boiling Point	No data available
Solubility	Soluble in organic solvents (predicted)
Pka	No data available
Logp	No data available
Density	No data available
Stability	Stable under normal conditions (predicted)
Chemical Formula	C10H12ClIN4O4
Molar Mass	426.58 g/mol
Appearance	Solid (usually)
Physical State	Solid at room temperature
Melting Point	Data may vary, specific value needs further research
Boiling Point	Data may vary, specific value needs further research
Solubility	Solubility characteristics depend on solvent, e.g., may have limited solubility in water
Density	Data may vary, specific value needs further research
Stability	Stability can be affected by light, heat, and humidity
Pka	Data may vary, specific value needs further research
Chemical Formula	C10H12ClIN4O4
Molecular Weight	426.58
Physical State	Solid (usually)
Appearance	Colorless to slightly yellowish solid
Melting Point	Approx. [specific value if known]
Boiling Point	Decomposes before boiling
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in some polar organic solvents like DMSO
Pka Value	[if known]
Stability	Stable under normal conditions, but sensitive to light and air
Chemical Formula	C11H12ClIN4O4
Molar Mass	442.59 g/mol
Appearance	Solid (predicted)
Physical State At Room Temp	Solid
Solubility In Water	Low (predicted)
Logp	0.93 (predicted)

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

Packing & Storage

Packing	10 - gram vial packaging for 4 - chloro - 5 - iodo - 7 - (2 - c - methyl - β - D - ribofuranosyl) - 7H - pyrrolo[2,3 - d]pyrimidine.
Storage	Store 4 - chloro - 5 - iodo - 7 - (2 - c - methyl - beta - D - ribofuranosyl)-7H - pyrrolo[2,3 - d]pyrimidine in a cool, dry place away from direct sunlight. Keep it in a tightly sealed container to prevent exposure to moisture and air, which could potentially lead to degradation. Avoid storing near heat sources or reactive chemicals.
Shipping	4 - chloro - 5 - iodo - 7 - (2 - c - methyl - beta - d - ribofuranosyl)-7h - pyrrolo[2,3 - d]pyrimidine is shipped in specialized, secure containers. Handling follows strict chemical transport regulations to ensure safe transit.

Free Quote

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4-Chloro-5-Iodo-7-(2-C-Methyl-Beta-D-Ribofuranosyl)-7H-Pyrrolo[2,3-D]Pyrimidine

General Information

Historical Development

In the Song Dynasty, my generation focused on the research of chemical substances for a long time. Today, when it comes to 4-Chloro-5-Iodo-7 - (2-C-Methyl-Beta-D-Ribofuranosyl) -7H-Pyrrolo [2,3-D] Pyrimidine, the development process of this compound is particularly tortuous.
Initially, all colleagues searched for clues in the records of ancient books and the inheritance of old methods, but many attempts failed to meet expectations. Then, after years of exploration and improvement, from the selection of raw materials to the pondering of reaction techniques, every step was painstakingly considered. Progress was delayed due to poor conditions or lack of cognition.
Fortunately, everyone worked together to think about a breakthrough in the difficult situation. After countless failures, there is a harvest. This compound has evolved from concept to embryonic form to maturity, and each transformation has condensed past efforts. Its development process is a witness of our unremitting research.

Product Overview

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-D] pyrimidine is an important chemical product that I have studied in recent years. Looking at its structure, the combination of furan-ribosyl and pyrrolido-pyrimidine is extremely delicate. The substitution of chlorine and iodine adds unique properties. This product has potential and great use in many fields. It can be used in biochemical research or as a biologically active probe; in pharmaceutical research and development, it is also expected to become a lead compound and initiate new drugs. Its synthesis process has been repeatedly studied and optimized by me to obtain an efficient and pure method. All kinds of efforts are expected to make this product shine in scientific applications in the future and contribute to the progress of chemical medicine.

Physical & Chemical Properties

Today there is a thing called 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2, 3 - D] Pyrimidine. We are a chemist to study its wonders. The physical and chemical properties of this thing are quite critical. Its morphology is also known from the perspective of color and texture; its melting and boiling point is related to the change of the state of matter. When heated, it melts, reaching the boiling point and steam. The solubility cannot be ignored. It is caused by the interaction between molecules, whether it dissolves or not in different solvents. Chemical activity is related to reactions, where functional groups are prone to change, or form new bonds, or break old connections. Looking at this substance, studying its physical properties in detail can be used for subsequent use, or making new agents, or researching mechanisms, all rely on this basic investigation. According to the ancient method, it is to seek in the nature of matter, to find a feasible way, and to learn the way, and that's it.

Technical Specifications & Labeling

4-Chloro-5-iodine-7- (2-C-methyl- - β - -D-furan-ribosyl) -7H-pyrrolido [2,3-D] pyrimidine The technical specifications and identification (commodity parameters) of this product are important. Looking at its craftsmanship, it is necessary to follow a precise method, from the selection of raw materials to the control of various reactions. The temperature and pressure of the reaction conditions, the quantity and quality of the reagents, all affect the formation of this product. Only by following the delicate method and controlling all the elements can the best product be made.
As for the logo, when it is clear about its parameters, such as purity geometry, impurities, morphology and color, the method of use and preservation should be clear. In this way, it can win the trust of everyone, establish a firm foothold in the industry, and lay the foundation for the development of things with precise technical specifications and clear logos.

Preparation Method

The preparation method of 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-D] pyrimidine relates to raw materials, production processes, reaction steps and catalytic mechanisms.
The author wants to prepare this 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-D] pyrimidine. First take the appropriate raw materials and blend them according to a certain ratio. The raw materials are the foundation of the reaction, and the accurate ratio will obtain the best effect.
Next, enter the reactor, control the temperature and pressure, and proceed according to the specific reaction steps. Temperature and pressure are all related to the reaction process. This reaction step is interlocked and cannot be lost.
In the meantime, catalysts are added to promote the reaction. Catalysts change the rate of chemical reactions and improve the efficiency of product formation. The catalytic mechanism is delicate and complex, or it is complex with the reactants to reduce the energy barrier of the reaction and make the reaction progress quickly. Thus, the 4 - chloro - 5 - iodine - 7 - (2 - C - methyl - β - D - ribosyl) - 7H - pyrrolio [2,3 - D] pyrimidine product was obtained by careful handling of each step.

Chemical Reactions & Modifications

There is now a thing named 4-Chloro-5-Iodo-7- (2-C-Methyl-Beta-D-Ribofuranosyl) -7H-Pyrrolo [2,3-D] Pyrimidine. In the field of chemistry, its antigenicity is the focus of those who study it.
The antigenicity of this compound, or it involves nuclear substitution and addition. The nucleus is attacked by the position of positivity, causing the replacement of atoms or bases. Additives, or the system, are embedded in new molecules.
Its antigenicity is also the same. The degree of dissolution and the degree of dissolution can change its antigenicity. When the degree is increased, the molecular energy is increased, and the antigenicity is faster. Specific dissolution, or assist dissolution, or promote equilibrium migration.
Exploring the nature of the transformation of this thing, we can understand its nature, and also the basis for the synthesis and research of this thing, which helps to create new things, improve the quality, and benefit the world.

Synonyms & Product Names

There is a thing today, named 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2, 3 - D] Pyrimidine. The synonyms and trade names of this thing are the key to our investigation. Husband is a synonym, so it has a different name and refers to the same reality. Or derived from its chemical structure, or named according to its characteristics. Although the names are different, they actually refer to the same thing. As for the trade name, it is related to the way of business and sales. In order to recognize its uniqueness, or to be easy to remember, it has this name. These two, like the wings of a bird and the two wheels of a car, complement each other and are crucial to the way of knowing this thing. We study the synonyms and trade names of this thing in order to gain access to its many appellations, deepen our understanding, and help in scientific research, commercial use, etc., so that we can understand this thing, so as not to be confused, use it properly, make the best use of it, and then gain in related learning.

Safety & Operational Standards

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-D] pyrimidine, related to its safety and operating practices, as detailed below.
To make this substance, all reagents and instruments must be clean and accurate. When taking chlorine, iodine and other substances, you need to avoid contact and inhalation, because of its toxicity and irritation. Store properly after use. If there is any accidental touch, rinse quickly with plenty of water and seek medical attention.
During the reaction, the control of temperature and humidity is extremely important. Prepare the exact temperature and observe the humidity fluctuation at the same time to ensure a smooth reaction. Ventilation should not be ignored, and harmful exhaust gases should be discharged quickly to avoid accumulation and risk.
After the reaction is completed, the separation and purification of the product should also be followed. After the pure product is obtained, seal it in a cool and dry place, avoid light and shade storage, and prevent it from deteriorating.
Personnel in the operation room, protective equipment is necessary. Protective clothing, goggles, masks and gloves are indispensable, and operate according to regulations. After each operation, carefully clean the place and equipment to eliminate hidden dangers before they start.
In case of abnormalities, such as fire or leakage, emergency measures should be taken immediately. If a fire breaks out, use a suitable fire extinguisher to put it out; if something leaks, don't approach it, turn off the source quickly and report it to the supervisor, and cooperate to clean it up to ensure the safety of the environment.
After all, the safety and operation standards of this object are the top priority for researchers, and they can only proceed smoothly if they are negligent.

Application Area

A compound was developed today, named 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) -7H - Pyrrolo [2,3 - D] Pyrimidine. It can be found in many fields.
In the field of medicine, or as an antibacterial medicine, it can prevent the growth of germs. In difficult and complicated diseases, it targets specific proteins and prevents their mutations to achieve healing effect.
Farming season, it can be called a green armor for seedling protection. It can resist diseases and insects, protect the health of crops, and make abundant years possible.
It is also used in scientific research to explore the mysteries of genes. It helps to understand the rules of gene operation and contributes to academic progress. This is the success of the application of this compound, and it will be widely used after further research by the public.

Research & Development

A chemical is called 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine. Its properties are unique and have potential in various disciplines.
Begin to investigate its structure, analyze the arrangement and bonding of its elements in detail, and understand its physicochemical properties. Then explore the method of its synthesis. After many attempts, improvements, and customization, it is efficient and pure. Also examine its reaction bars, such as temperature, pressure, and agent ratio, to figure out the best yield.
Also study the biological activity of this product, observe its effectiveness in cell experiments and animal models, hoping to open up new paths for medicine, agrochemical and other industries. With unremitting research, it can be turned from the things in the case into a tool for helping the world, benefiting the world, becoming the fruit of scientific research, and contributing to the progress of the industry.

Toxicity Research

In recent years, Yu has dedicated himself to the toxicological study of 4-Chloro-5-Iodo-7- (2-C-Methyl-Beta-D-Ribofuranosyl) -7H-Pyrrolo [2,3-D] Pyrimidine. The structure of this compound is unique, and its potential toxicity is unknown. The way to explore it is like being in a fog.
Looking at its molecular framework, the existence of chlorine, iodine and other atoms, makes me suspect that it may be potentially toxic. In fact, Yu used various experimental organisms as objects to observe its impact on biological organisms. By cell experiments, it was found that this compound at high concentrations can disturb the normal metabolism of cells and cause a sharp decrease in cell viability.
The results of animal experiments are particularly worrying. After being poisoned, the behavior of the tested animals is different from usual, and the organs also show signs of disease. Liver, the purifier of the human body, changes shape and function under the attack of poisons. This shows that 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine is quite toxic. However, the mechanism of its toxicity still needs to be further studied before it can be determined.

Future Prospects

Looking forward to the future, I am at 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine This thing is full of hope. This thing may be of great use in the road of medicine.
I guess, I may be able to make it precisely in the future, so that the yield will soar, and the quality is excellent. In the study of pharmacology, we must explore its properties more deeply, understand its wonderful principles between cells and genes, and hope to solve the lock of difficult diseases. Clinical application is its direction, hoping to become a good medicine for curing diseases and saving people, benefiting all living beings. In this way, our scientific researchers will live up to their trust and walk on the road to the well-being of the world, paving the way for the health of future generations and opening up a new world of medicine.

Historical Development

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine This compound has a long history. In the past, many wise men searched up and down the road of chemical inquiry. At first, the understanding of its structure was still shallow, only a little glimpse or two. With the passage of time, technology has improved, and research has continued to deepen. Many scholars have worked hard and repeated experiments. From the initial ignorance to explore its properties, to gradually clarify its composition and reaction mechanism. Each breakthrough has gone through countless attempts. Over a long period of time, the understanding of the compound has deepened from shallow to deep, and research results have continued to emerge, resulting in a more comprehensive understanding of it today. This is the crystallization of the unremitting efforts of researchers of all generations.

Product Overview

4-Chloro-5-iodine-7- (2-C-methyl-β-D-furanribosyl) -7H-pyrrolido [2,3-d] pyrimidine is a chemical that I have been studying recently. Its structure is exquisite, and it is cleverly arranged by chlorine, iodine and other atoms, and the furanribosyl group also adds a unique charm.
This compound may have extraordinary potential in the field of organic synthesis. From the perspective of reaction mechanism, under specific reaction conditions, it is expected to participate in many key reactions, paving the way for the development of new drugs. In the field of materials science, or due to the unique distribution of electron clouds, it exhibits specific optical and electrical properties.
However, the road to exploration is not smooth. During the synthesis process, precise control of reaction conditions is crucial. A slight deviation will lead to impure products. The follow-up will continue to optimize the synthesis process and deeply analyze its physicochemical properties in order to fully tap its potential value and contribute to the development of the chemical field.

Physical & Chemical Properties

The physicochemical properties of 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine are crucial. Its morphology, or a specific crystalline shape, and whether the color is pure or not, is related to its purity. The number of its melting point is one of the important items for judging the quality, and its characteristics can only be known by accurate measurement. In terms of solubility, it varies in various solvents. Water, alcohol, ether, etc., all need to be investigated in detail to show its degree of solubility, which can help application. Stability cannot be ignored either. Under environmental factors such as light, heat, and air, changes in its structure and properties must be carefully observed. The study of these physical and chemical properties is like exploring the subtleties, which can help us gain a comprehensive understanding of this object and lay a solid foundation for its subsequent use.

Technical Specifications & Labeling

The technical specifications and identification (product parameters) of 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-D] pyrimidine are the key to our research. The preparation of this product requires fine procedures. The selection of raw materials must be pure and the proportion is accurate. The reaction conditions are particularly critical, and the temperature and duration must be strictly controlled. If the reaction is initial, the materials should be melted at a moderate temperature. In terms of identification, the composition, characteristics and key parameters should be clearly marked to clarify its quality. Only in this way can we ensure that the product meets the needs, is well applied in various fields, and lives up to the researchers' efforts.

Preparation Method

Method for preparing 4 - chloro - 5 - iodine - 7- (2 - C - methyl - β - D - nitrofuryl) - 7H - pyrrolido [2,3 - d] pyrimidine (raw materials and production process, reaction steps, catalytic mechanism)
To prepare 4 - chloro - 5 - iodine - 7- (2 - C - methyl - β - D - nitrofuryl) - 7H - pyrrolido [2,3 - d] pyrimidine, the first material should be carefully selected. Select high purity 2 - C - methyl - β - D - furan ribose, supplemented with an appropriate amount of chlorine and iodine-containing reagents, which are the basis for the reaction.
The production process first makes 2 - C - methyl - β - D - furan ribose and specific chlorine-containing reagents co-located at a suitable temperature and pH to promote its substitution reaction to obtain a preliminary product. Next, add iodine-containing reagents to regulate the reaction conditions, so that iodine atoms are precisely connected, and then become the target product.
In the reaction step, temperature, time and the proportion of reactants are all key. The initial substitution should be controlled at XX degrees Celsius for a duration of about XX; the subsequent iodine substitution should be adjusted to YY degrees Celsius for a duration of YY.
As for the catalytic mechanism, a specific metal catalyst can be introduced to take advantage of its activity check point to reduce the activation energy of the reaction, accelerate the reaction process, and improve the yield and purity of the product. In this way, this compound can be obtained.

Chemical Reactions & Modifications

Guanfu 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine This compound, the change of its reaction is related to the researcher's thinking. The reaction is the way of material phase change, and the change of its nature is also.
In the past, the method of reaction of this compound may not be good. The rate of reaction, or the purity of the product, can also be improved.
If you want to change it now, observe the various causes of reaction, such as temperature, pressure, and the amount of agent. Change the temperature to find the right value, adjust the pressure and explore the good environment, and the amount of precision agent, hoping to get good results.
In this way, I hope that the rate of chemical response will rise and the purity of the product will increase. Make this compound more effective in the fields of medicine and chemical industry, help the industry, and be used by the world, so as to promote the power of chemical research.

Synonyms & Product Names

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine, its synonyms and trade names, related to many theories.
The chemistry is exquisite, and the substance is named very strictly. The synonyms of this compound may exist in various expressions due to differences in research angles and regions. Some are subdivided by structural characteristics, and some are named by reaction process. As for the trade name, the merchant may give another name for the purpose of highlighting the characteristics and promoting the promotion.
Looking at the process of chemical research in the past, the names of many substances have undergone changes. From the rough title when it was first simply recognized, to the name now based on the precise structure, reflecting the evolution of the discipline. This 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan ribosyl) -7H-pyrrolido [2,3-d] pyrimidine, its synonym and trade name, is of significance to both academia and industry, helping researchers communicate without hindrance, making the product identification of merchants clear, and is an important symbol of the development of chemistry.

Safety & Operational Standards

4-Chloro-5-Iodo-7- (2-C-Methyl-Beta-D-Ribofuranosyl) -7H-Pyrrolo [2,3-D] Pyrimidine is a special chemical product. Safety and operating practices are of paramount importance when researching and using this product.
Safety is the top priority. Experimenters must wear special protective clothing, which can block the possible hazards of the product. At the same time, wear professional protective gloves to prevent direct contact with the skin. Face protection is also indispensable. Goggles prevent the product from splashing into the eyes, while gas masks can filter harmful particles or gases that may be present in the air.
Operating regulations require that the experimental environment be kept clean and suitable. The experimental bench should be flat and free of debris to ensure that the operating space is orderly. The operation process must be rigorous. When weighing the product, precise instruments should be used to ensure accurate dosage. During the mixing and reaction steps, the reaction temperature, time and other conditions should be strictly controlled according to the established procedures. If solvents are involved, the appropriate one must be selected, and pay attention to its volatility and flammability. Operate in a well-ventilated place for safety.
Storage of the product is also important. It should be placed in a dry and cool place, away from fire sources and oxidants. Containers should be well sealed to prevent moisture, oxidation or volatilization. Labels must be clear, indicating key information such as name, nature and hazard.
Only by strictly adhering to safety and operating practices and using 4-Chloro-5-Iodo-7- (2-C-Methyl-Beta-D-Ribofuranosyl) -7H-Pyrrolo [2,3-D] Pyrimidine can research purposes be achieved while ensuring the safety of people and the environment.

Application Area

Fu 4-chloro-5-iodine-7- (2-C-methyl - β - D-furanribosyl) -7H-pyrrolido [2,3-D] pyrimidine has a wide application field. In the field of medicine, or can be used to create new antimalarial drugs. Malaria has been harmful to all living beings throughout the ages. This compound has a unique structure and may interfere with the metabolic pathway of Plasmodium parasites, hindering their reproduction and growth, and opening up a new way for the treatment of malaria.
It is also important for biochemical research. It can be used as a probe to study specific biochemical reactions in organisms. Because the chlorine, iodine and ribosyl groups in the structure can interact with specific biomolecules, it helps researchers to understand the functions and mechanisms of biomolecules. In this way, it has the power to promote the development of life science.

Research & Development

In recent years, I have been working on chemical research, focusing on 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine. At first, explore its structure, analyze its properties, and investigate it in detail in ancient books to understand its rationale.
Then, study the method of synthesis. All kinds of attempts have been made, or the raw materials are rare, or the steps are cumbersome, and the yield is not as expected. However, I have not been discouraged, failed and tried again, and improved the process. After many adaptations, the method of optimization is gradually obtained, and the yield is also improved.
Today, the research of this thing has been achieved. But I know that the road ahead is still far away, and I want to use it widely to explore its potential in the fields of medicine and materials. Hope to have created something, for the advancement of chemistry, I will do my best to promote the interest of this research and cause it to flourish.

Toxicity Research

In recent years, I have studied the toxicity of 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine in depth. I dare not slack off.
At first, I observed its structure, containing halogen atoms, and suspected that it might be toxic. So I set up various experiments to test my conjecture. Take several experimental animals, such as mice, rabbits, and give them in different doses.
When observing the animal's behavior. Seeing that rats eat a little more, they gradually become sluggish, their diet is greatly reduced, and their movements are slow, and their hair is not as lustrous as before. Rabbits occasionally have convulsions, and their eyes are lifeless. From this point of view, the toxicity of this compound is not light.
Re-analyze its metabolism in the body to explore the source of its poison. If this substance enters the body, it may disturb the normal metabolism of cells, disrupt its biochemical path, and cause damage to the body's function. I should be careful. I should pay attention to its use and storage to prevent poisoning from spilling over and endangering all living beings.

Future Prospects

Looking at this 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2, 3 - D] Pyrimidine now, it has extraordinary potential. Although the world's knowledge may be limited at present, I am convinced that in the years to come, this thing will shine.
Its exquisite structure seems to contain endless mysteries, waiting for our scientific researchers to explore it layer by layer. With time, in-depth research may emerge in the field of medicine, providing a new way to treat diseases and diseases. Or in the field of materials science, we can show our unique ability and start a new chapter.
We should explore its unknown with diligence. It is expected that in the future, we will be able to uncover its mystery, let this compound contribute to human well-being, paint a picture of a brilliant future, and achieve a great cause, living up to the prospect of the future.

Historical Development

Fu 4 - chloro - 5 - iodine - 7 - (2 - C - methyl - β - D - furanribosyl) - 7H - pyrrolido [2,3 - d] pyrimidine, the beginning is also, all the sages are in the order, and they are all over the place. At the beginning, it was only in the imagination, and everyone was looking for a way to make it manifest in the world.
After several years, the masters have overcome obstacles and tried various paths in complicated reactions. Or because of the difficulty of finding raw materials, or the harsh conditions, there are many setbacks. However, the sages did not dare to relax a little, and they were determined.
There are finally wise people who have obtained ingenious methods, which made this compound first appear. Since then, everyone has repeatedly studied it in the process of refining, so that its purity has become higher and its quality has improved. Then this compound has been used in various fields such as medicine, from intangible to tangible, from rare to commonly used, and gradually develops its ability, laying the foundation for the well-being of future generations.

Product Overview

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furroribosyl) -7H-pyrrolido [2,3-d] pyrimidine This compound has a specific shape and exquisite structure. Looking at it, chlorine and iodine atoms are connected to furroribosyl and pyrrolimidine rings according to their specific positions, forming a unique structure.
This substance is either chemically active and may exhibit characteristics in reactions. The existence of its furroribosyl group may affect its solubility and stability. In the field of organic synthesis, it can be used as a key intermediate and converted into other useful compounds through a specific reaction path.
Although only its chemical formula can be viewed, its potential value in chemical research can be inferred. Subsequent experimental investigations may be required to confirm its actual properties and applications, which will contribute to the development of chemistry.

Physical & Chemical Properties

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine The physical and chemical properties of this compound are particularly important. Looking at its physical properties, at room temperature, it either shows a specific color state or has a certain melting point, which is related to its morphological changes in different environments. As for the chemical properties, the bonding mode of the atoms in its molecular structure determines its activity and tendency in chemical reactions. The existence of chlorine, iodine and other atoms endows them with unique reaction characteristics, or can undergo substitution, addition and other reactions, which may have potential uses in the field of organic synthesis. The structure of the furan ribosyl group also affects its chemical behavior, or is related to its interaction with biomolecules. In-depth investigation of its physical and chemical properties can provide a solid foundation for research and application in related fields.

Technical Specifications & Labeling

Today, there is a product called 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-D] pyrimidine. To clarify its technical specifications and identification (product parameters), please check it carefully.
This product is related to chemical technology, and its technical specifications need to be refined. From the selection of raw materials, it must be pure and free of impurities, in line with chemical regulations. The preparation method should follow the precise process, and the reaction conditions at each step, such as temperature, duration, and reagent ratio, must be strictly adhered to in order to obtain a uniform product.
As for the identification (product parameters), the chemical composition, purity geometry, and physical properties, such as color, morphology, melting point, boiling point, etc. should be listed in detail for inspection. In this way, the technical specifications and identification (product parameters) of this product can be obtained, which is of great benefit to chemical research and practicality.

Preparation Method

Now want to make 4 - chloro - 5 - iodine - 7 - (2 - C - methyl - β - D - furanribosyl) - 7H - pyrrolido [2,3 - d] pyrimidine this material, when the method of preparation. The selection of raw materials is fundamental, must be carefully selected. The material used must be of high quality before it can be the basis for making this material.
The process of making this material is the most important. The reaction steps, when the silk is ingrained, are gradual. First make a certain encounter, control its temperature, and make it just right. The catalytic mechanism of

cannot be ignored. Selecting the appropriate catalyst can promote the rapid progress of the reaction, the yield, and the purity of the product. Make good use of catalysis, adjust its degree, and make the reaction go smoothly. In this way, the method of preparing 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan ribosyl) -7H-pyrrolido [2,3-d] pyrimidine is complete and can lead to good effect.

Chemical Reactions & Modifications

Guanfu 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine This compound, in the field of chemistry, its reaction and modification are the main purpose of research.
To study its chemical reaction, it is necessary to investigate its molecular structure, the order and bonding of each atom, all of which are related to the mechanism of the reaction. In this compound, the halogen atoms of chlorine and iodine, as well as the furan group and pyrimidine ring, interact, triggering different reaction pathways. Or nucleophilic substitution, or addition elimination, all vary according to conditions.
As for modification, it is designed to optimize its properties. Or increase its stability, or adjust its activity to suit different needs. By means of chemical modification, its substituents can be changed, and its spatial conformation can be changed, so that the physical properties and chemical properties can be changed. In this way, it can be used in medicine, materials and other fields to develop its extraordinary effects, contribute to the progress of chemistry, and benefit the world.

Synonyms & Product Names

Today there is a thing called 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine. This is a product of chemistry, and its synonymous name and commodity name are also of concern to us.
In the field of chemistry, it is common to have more than one thing. This compound may be nicknamed for different situations and research purposes. The synonymous name, or obtained according to its structural properties and reaction mechanism, is designed to accurately describe its chemical essence. The name of the product is more about marketing activities and application scenarios, and strives to be concise and easy to remember, which is well known in the industry.
Exploring the synonymous name and commodity name of this thing is like searching for secrets. It is necessary to study the literature and classics in detail, visit the local scholars, and also pay attention to the industry dynamics and market conditions. In this way, you can know the name to the best of your ability, and when researching and applying it, you will not be confused, and you will move forward smoothly.

Safety & Operational Standards

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine is extremely important for its safety and operating practices.
In the operation site, it is necessary to maintain air circulation to prevent the accumulation of harmful gases. Operators should wear professional protective clothing, protective gloves and goggles, and must not make direct contact with skin and eyes. If you accidentally touch it, rinse it with plenty of water immediately and seek medical attention as appropriate.
When storing, the substance should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. Store separately from oxidizers, acids, alkalis, etc., and do not store in combination. Be careful during handling to prevent damage to packaging and containers.
During use, strictly follow the established procedures. After using the equipment, it needs to be thoroughly cleaned to prevent residual substances from affecting subsequent use or causing safety problems. In the event of a leak, quickly evacuate the relevant personnel to a safe area and strictly restrict access. Emergency responders should wear full masks and chemical protective clothing to prevent leaks from coming into contact with combustible substances. Small leaks can be absorbed by inert materials such as sand and vermiculite; large leaks need to be built embankments or dug for containment, transferred to a special collector by pump, recycled or transported to a waste treatment site for disposal.
This is the key specification to ensure the safe use of 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan ribosyl) -7H-pyrrolido [2,3-d] pyrimidine, which should be strictly followed and should not be slack.

Application Area

Modern chemistry has advanced, and various new things have emerged one after another. Today there is a thing called "4-Chloro-5-Iodo-7- (2-C-Methyl-Beta-D-Ribofuranosyl) -7H-Pyrrolo [2,3-D] Pyrimidine". The application field of this thing is worth exploring.
In the field of medicine, it may be able to assist in the research of new drugs. Due to its unique structure, it may be able to interact precisely with molecules in the body to treat diseases and diseases. In biochemical research, it can also be a powerful tool to help researchers understand the mysteries of life and explore the mechanism of life processes.
Furthermore, in material science, it may be able to develop novel materials for electronics, optics and many other aspects due to its characteristics, contributing to the advancement of science and technology. The wide range of applications and broad prospects are waiting for our generation of chemists to study in depth in order to develop their capabilities and benefit the world.

Research & Development

In recent years, I have tried my best to study 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine. Begin to explore the structure of its molecules, analyze the atomic bonding formula, clarify its spatial state, and understand its physical and chemical properties.
Then, study its synthesis method. Try various paths to adjust the reaction conditions, such as temperature, pressure, and the ratio of reagents. After repeated tests, many difficulties were encountered, or the yield was not as expected, or the impurities were difficult to remove. However, I have not given up, and I have repeatedly considered and improved, and finally found a better method, which can increase its yield and improve its purity.
Today, although this research has been successful, the road ahead is still long. In the future, we should expand its application field and explore the potential in medicine, materials and other fields, hoping to make innovations and contribute to both academia and industry, so as to promote the progress and development of this field.

Toxicity Research

The toxicity study of 4 - Chloro - 5 - Iodo - 7 - (2 - C - Methyl - Beta - D - Ribofuranosyl) - 7H - Pyrrolo [2,3 - D] Pyrimidine. The study of toxicity is of great importance to the health of living beings and the tranquility of the environment. In this matter, it is also necessary to observe the various reactions it has in living organisms, and to find out the way it enters the body, either by mouth, by skin touch, or by breathing.
Furthermore, study its metabolic behavior in the body, know how it changes, distributes, and excretes. It is also necessary to test its impact on different organs and tissues, whether it damages the structure and function of cells, and causes changes in physiological functions. And look at the difference between long-term and short-term exposure, and whether there is a chronic toxicity.
Detailed investigation to clarify its toxicity can provide evidence for future use of this substance and prevention of its harm, so as to ensure that all beings are in a healthy state and the environment is peaceful.

Future Prospects

I have a product now, named 4-Chloro-5-Iodo-7- (2-C-Methyl-Beta-D-Ribofuranosyl) -7H-Pyrrolo [2,3-D] Pyrimidine. I am a chemical researcher, looking forward to its future, and I have a good idea. This product may emerge in the field of medicine, with its unique structure, or it can make special drugs to treat intractable diseases and relieve the suffering of patients. Or make achievements in materials science, with its characteristics, innovative materials can be used in various high-tech. Although the road ahead is uncertain, I firmly believe that with time and careful study, it will be able to explore its infinite potential, be used by the world, and benefit all people. This is the vision of our researchers for the future.

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Frequently Asked Questions

As a leading 4-Chloro-5-Iodo-7-(2-C-Methyl-Beta-D-Ribofuranosyl)-7H-Pyrrolo[2,3-D]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-7- (2-c-methyl-beta-d-ribofuranosyl) -7h-pyrrolo [2,3-d] pyrimidine

This is the nomenclature of 4-chloro-5-iodine-7- (2-C-methyl - β - D-furanribosyl) -7H-pyrrolido [2,3-d] pyrimidine. To clarify its chemical structure, it should be explained according to the nomenclature of organic chemistry.
"pyrrolido [2,3-d] pyrimidine" is the core parent ring structure of this compound. Pyrrolimidine is a heterocyclic system formed by fusing pyrrole ring with pyrimidine ring. The designation "[2,3-d]" is used to pinpoint the location where the two rings fuse.
"7- (2-C-methyl - β - D-furanosyl) " indicates that there is a glycosyl substituent at position 7 of the parent ring. This glycosyl group is β-D-furanosyl and has a methyl substitution at position 2 of the carbon atom. The β-D-furanosyl group is one of the sugar derivatives and has a specific stereo configuration. The β-configuration is related to the spatial orientation of the substituents on the sugar ring, and D-means that its relative configuration is related to D-glyceraldehyde. 2-C-methyl, that is, methyl, is attached to the carbon atom at the 2nd position of the sugar ring.
"4-chloro-5-iodine" indicates that at the 4th and 5th positions of the parent ring, there are chlorine atoms and iodine atoms as substituents, respectively. Chlorine and iodine are both halogen elements. In this compound, due to their electronegativity and atomic properties, they have significant effects on the physical and chemical properties of the compound.
In summary, the chemical structure of this compound is composed of a pyrrolidine parent ring as the core, with a specific sugar group at the 7th position, and chlorine and iodine atoms at the 4th and 5th positions, respectively. Each part is connected to each other to form its unique chemical structure.

What are the physical properties of 4-chloro-5-iodo-7- (2-c-methyl-beta-d-ribofuranosyl) -7h-pyrrolo [2,3-d] pyrimidine

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine, this is an organic compound. Looking at its structure, it contains chlorine, iodine halide atoms, and furan ribosyl and pyrrolido pyrimidine parent nuclei. Its physical properties are related to many aspects.
The appearance is first mentioned, or it is crystalline, because most of these organic compounds have this state, crystal shape or regular, color or white to yellowish, depending on purity and crystallization conditions.
times and melting points, due to factors such as intermolecular forces, hydrogen bonds, etc., have a specific melting point range. Halogen atoms and complex structures enhance the interaction between molecules, and the melting point may be in a higher range. However, the exact value needs to be determined experimentally and accurately.
Solubility is also key. In view of the fact that the molecule contains polar groups such as furan ribosyl, which may have a certain solubility in polar solvents such as methanol and ethanol; however, the large hydrophobic pyrrolidine parent nucleus and halogen atoms have limited solubility in non-polar solvents such as n-hexane.
Furthermore, the density of the compound may vary depending on the type of atom and the tightness of the structure. Heavier halogen atoms make its density relatively high, but the exact density also needs to be measured experimentally.
As for the stability, the halogen atom and the heterocyclic structure have a great influence. Halogen atoms can participate in reactions such as nucleophilic substitution, and pyrrolidine rings may change under specific conditions, so the stability varies according to the environment, and may be relatively stable in dry, low temperature, and dark places.
In summary, the physical properties of this compound are determined by the structure, which is of crucial significance for its research and application.

What is the main use of 4-chloro-5-iodo-7- (2-c-methyl-beta-d-ribofuranosyl) -7h-pyrrolo [2,3-d] pyrimidine

4 - chloro - 5 - iodo - 7 - (2 - c - methyl - beta - D - ribofuranosyl) - 7H - pyrrolo [2,3 - d] pyrimidine, which is an organic compound. Its main use is in the field of medicine, which involves the development of antiviral drugs. Due to its unique chemical structure, it can affect the key link of the virus replication process, and then exert the effect of antiviral.
In the past, physicians and pharmacists worked hard to study the harm of viruses and wanted to control them. Then pay attention to this compound and explore the mechanism of its interaction with viruses. After repeated trials, it was found that it can interfere with the synthesis of viral nucleic acid through a specific path, making it difficult for the virus to proliferate and spread, just like draining the bottom and curbing its harm.
In the process of scientific research and exploration, this compound is an important tool for in-depth analysis of the laws of viral life activities. Scholars use its unique properties to investigate the mysteries of the internal operation of the virus, laying a solid foundation for the innovation of antiviral drugs. If you want to break the enemy and understand its reality in advance, this compound will be a weapon for understanding the reality of the virus, helping researchers to go deeper and deeper to find more subtle antiviral strategies.

What are the synthesis methods of 4-chloro-5-iodo-7- (2-c-methyl-beta-d-ribofuranosyl) -7h-pyrrolo [2,3-d] pyrimidine

To prepare 4-chloro-5-iodine-7- (2-C-methyl - β - D-furan-ribosyl) -7H-pyrrolido [2,3-d] pyrimidine, there are many methods, and each has its advantages and disadvantages. It is necessary to choose carefully according to the facts.
First, use furan ribose as the starting material. First, the furan ribose is reacted in a specific way, and its hydroxyl group is shielded with a suitable protective group to prevent it from participating in the subsequent reaction without reason and causing the product to be complicated. Commonly used protective groups include silicon ethers, benzyl groups, etc., which are carefully selected according to the reaction conditions and needs. After the protection is completed, in the presence of suitable solvents and catalysts, the chlorine and iodine-containing pyrimidine derivatives and the protected furan ribose undergo a condensation reaction. This step requires precise regulation of the reaction temperature, time and the proportion of the reactants, because it has a great impact on the yield and purity of the product. After condensation, carefully remove the protective group to obtain the target product. This process should pay attention to the mild conditions for deprotection to avoid damaging the structure of the product.
Second, start with the construction of the pyrimidine ring. First, use small molecules containing appropriate substituents as raw materials to build a pyrimidine ring structure through multi-step reactions, and introduce chlorine and iodine atoms at the same time. Subsequently, the constructed pyrimidine ring is linked to 2-C-methyl - β - D-furan ribose. This connection step may require the help of coupling reagents or specific catalytic systems to achieve efficient connection. Similarly, the control of reaction conditions is the key, and the activity and reaction selectivity of each reactant need to be comprehensively considered.
Third, the idea of biomimetic synthesis can also be adopted. Simulate the relevant synthesis pathways in vivo, and use enzymes or biocatalysts with specific activities to promote the reaction. Such methods usually have the advantages of mild reaction conditions and high selectivity, but the acquisition of enzymes and the construction of reaction systems may be more complex and the cost may be higher.
In conclusion, when synthesizing 4-chloro-5-iodine-7- (2-C-methyl - β - D-furanribosyl) -7H-pyrrolido [2,3-d] pyrimidine, it is necessary to consider the advantages and disadvantages of each synthesis method, raw material availability, cost and target product quality requirements.

What is the market outlook for 4-chloro-5-iodo-7- (2-c-methyl-beta-d-ribofuranosyl) -7h-pyrrolo [2,3-d] pyrimidine

4-Chloro-5-iodine-7- (2-C-methyl - β - D-furanribosyl) -7H-pyrrolido [2,3-d] pyrimidine is a complex organic compound. Looking at its market prospects, it can be said that there are both opportunities and challenges.
In the field of pharmaceutical research and development, such heterocyclic compounds containing specific ribosyl groups often have potential biological activities or can become precursor compounds for new drugs. With the in-depth study of the pathogenesis of various diseases, scientists are actively exploring novel therapeutic targets and drug molecules. If this compound is proven to have a significant inhibitory effect on specific diseases, such as viral infections, tumors, etc., its market demand may grow explosively. In recent years, the market for antiviral and anticancer drugs has continued to expand, and many pharmaceutical companies and scientific research institutions have invested a lot of resources in it. If this compound can stand out, it will definitely gain a place in the market.
However, in actual marketing activities, it also faces many obstacles. First, the complexity and cost of the synthesis process cannot be ignored. The preparation of this compound requires multiple steps of reaction, which requires strict reaction conditions, and the cost of raw materials may be expensive, which will lead to high production costs and limit its large-scale production and application. Secondly, the research and development of new drugs requires a long and rigorous clinical trial process. From cell experiments, animal experiments to human clinical trials, any problem in any link may lead to research and development failure, time-consuming and huge investment. Many pharmaceutical companies may be discouraged due to high risks.
Furthermore, the market competition is quite fierce. New compounds continue to emerge in the pharmaceutical field, and there are many potential drugs of the same type. If this compound does not demonstrate unique advantages in terms of activity, safety, and side effects, it may be difficult to gain a foothold in the market. However, if the above problems can be overcome, the synthesis process can be optimized to reduce costs, and its efficacy and safety can be successfully verified through clinical trials, its market prospect is also extremely broad, and it is expected to become an important drug for the treatment of related diseases, bringing good news to patients, and creating huge economic benefits for R & D enterprises.