(S)-2-(3-Iodophenyl)Pyrrolidine

Fengxi Chemical

Specifications

HS Code	528429
Chemical Formula	C12H14IN
Molecular Weight	299.15
Appearance	Solid (usually)
Physical State At Room Temp	Solid
Melting Point	Varies (needs experimental determination)
Boiling Point	Varies (needs experimental determination)
Solubility In Water	Low (organic compound, likely sparingly soluble)
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform
Density	Needs experimental determination
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula	C10H12IN
Molecular Weight	287.11
Appearance	Solid (Typical)
Solubility In Water	Low (due to non - polar nature of the phenyl and pyrrolidine rings)
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform, etc.
Chirality	Exists in (S)-enantiomer form as specified, has chiral center at the 2 - position of pyrrolidine ring
Reactivity	Iodo group can participate in substitution reactions, pyrrolidine ring can be involved in nucleophilic or basic - catalyzed reactions

As an accredited (S)-2-(3-Iodophenyl)Pyrrolidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of (s)-2-(3 - iodophenyl)pyrrolidine packaged in a sealed plastic container.
Storage	(s)-2-(3-iodophenyl)pyrrolidine should be stored in a cool, dry place, away from direct sunlight. Keep it in a tightly sealed container to prevent moisture and air exposure, which could potentially cause degradation. Store it separately from incompatible substances, such as strong oxidizing agents. Follow all safety guidelines to ensure its stability and integrity during storage.
Shipping	( S ) -2-(3 -iodophenyl)pyrrolidine is shipped with strict adherence to chemical transportation regulations. It's carefully packaged to prevent breakage and leakage, ensuring safe transit to the destination.

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General Information

Historical Development

(S) 2- (3-Iodophenyl) Pyrrolidine is also an organic compound. Looking back at its historical evolution, at the beginning, organic chemistry was still ignorant, and its research was only scratchy. However, the heart of a scholar, like the incessant fire, has deepened.
In the past, it was limited to skills, and it was difficult to obtain this compound. All kinds of attempts, but many came to nothing. But over time, chemical skills have become more and more exquisite. New reaction mechanisms have gradually become apparent, and new synthesis methods have been introduced.
Chemists have been working hard in the laboratory for many years. Or improve the old method, or create a new path. After countless setbacks, they are still determined. Finally, the synthesis of (S) -2- (3-Iodophenyl) Pyrrolidine became standardized and the yield increased step by step. Its historical evolution is a witness to the wisdom and perseverance of chemists, and a vivid chapter in the development of organic chemistry.

Product Overview

(S) 2- (3-iodophenyl) pyrrolidine is a valuable compound in the field of organic synthesis. Its unique structure is based on pyrrolidine ring, and 3-iodophenyl is cleverly connected to the second position of pyrrolidine. This compound has great potential in many chemical research fields, such as medicinal chemistry and materials science.
In pharmaceutical chemistry, due to its specific structure, it can be used as a key intermediate, modified and transformed to generate novel drug molecules with unique biological activities. In the field of materials science, it may be able to participate in the construction of specific materials and endow materials with novel properties.
Synthesis of this compound requires fine chemical operation, attention to reaction conditions, raw material ratio and reaction process to ensure product purity and yield. In-depth research on it may open up new paths for chemical innovation and development, and promote progress in related fields.

Physical & Chemical Properties

(S) 2- (3-Iodophenyl) Pyrrolidine is also an organic compound. Its physical and chemical properties are related to the characteristics of this compound and cannot be ignored. Its color state is either solid or liquid, depending on the conditions of temperature and pressure. Its melting point and boiling point can determine the temperature point of its phase transition. Solubility is related to its affinity for various solvents. In water, alcohol, ether and other solvents, the solubility varies. Its chemical activity is also a key feature. The iodine atom and pyrrolidine ring on the benzene ring can initiate various chemical reactions. Nucleophilic substitution and coupling reactions are all possible. This compound is a key intermediary in the field of organic synthesis, and the exploration of its physical and chemical properties is really helpful for the improvement of the organic synthesis process.

Technical Specifications & Labeling

(S) 2- (3-Iodophenyl) Pyrrolidine is an important organic compound. Its preparation process is crucial. When synthesizing this compound, strict technical specifications need to be followed. The selection of raw materials should be accurate, and the reaction conditions should also be carefully controlled. Commodity parameters such as temperature, reaction time and proportion of reactants all have a significant impact on the purity and yield of the product.
In terms of technical specifications, the synthesis steps should be carried out in an orderly manner, and each step of the reaction must be strictly separated and purified to ensure the removal of impurities. The identification of the product requires a variety of analytical methods, such as nuclear magnetic resonance, mass spectrometry, etc., to accurately determine its structure and purity, in order to ensure that (S) 2- (3-Iodophenyl) Pyrrolidine meets the corresponding Quality Standards and meets the needs of subsequent scientific research or production.

Preparation Method

The method of making (S) -2- (3-iodophenyl) pyrrolidine is related to the raw materials and production process, reaction steps and catalytic mechanism. First, an appropriate amount of starting materials is taken and put into the reactor in a precise ratio. The starting material needs to be strictly purified to maintain purity.
The reaction steps are as follows: First, the raw materials are mixed at a specific temperature and pressure to initiate a preliminary reaction. At this stage, the temperature should be controlled within a certain range, such as [X] degrees Celsius, the pressure is about [X] Pa, and it lasts for [X] hours to achieve the initial conversion.
The catalytic mechanism is crucial, and a specific catalyst, such as [specific catalyst name], is selected to promote the efficient progress of the reaction. This catalyst can reduce the activation energy of the reaction and speed up the reaction rate.
In the production process, attention should be paid to the cleanliness of the reaction environment and the avoidance of impurities. And during the reaction process, timely monitoring is required to fine-tune the reaction conditions according to the monitoring results to ensure the high yield and purity of the product. In this way, (S) 2- (3-iodophenyl) pyrrolidine can be prepared.

Chemical Reactions & Modifications

In recent years, the chemical product has been studied in the product of (S) -2- (3-Iodophenyl) Pyrrolidine, which has taken a lot of effort. The rules of its adaptation were not clear at the beginning, resulting in little effect.
Looking at various ancient books and trying to imitate the ancient method, but the reaction is mostly stagnant. For this reason, because the conditions are not suitable, the reactants are not properly matched, and the temperature and pressure are not suitable.
Then think about the method of change, adjust the proportion of the material, control the temperature and pressure. It is also easy to catalyze, hoping to get good results.
After repeated testing, it gradually turns around. The reaction rate increases slightly, and the purity of the product also rises. This is the work of transformation. Although it is not perfect, it has seen hope. In the future, we should be more diligent to ensure that the transformation of this product reaches an exquisite state and adds bricks and tiles to the chemical industry.

Synonyms & Product Names

Today there is a thing named (S) -2- (3-Iodophenyl) Pyrrolidine. This is a product of chemistry and has attracted much attention in my chemical research. Its synonyms and trade names are also the key to investigation.
Looking for its synonyms, if you want to explore it in detail, you need to study classics and literature in detail. Each synonym is like a secret clue, leading us to understand the characteristics and origins of this thing in depth. Many synonyms are born due to different reaction paths, or due to the naming preferences of the discoverers.
As for the trade name, it is related to the circulation of this thing in the market. Different merchants have another name for the product in order to recognize its uniqueness, or according to the characteristics and uses of the product. This reflects the diverse market demand for (S) -2- (3-Iodophenyl) Pyrrolidine, and is also a window for us to gain insight into industry trends. A detailed study of synonyms and trade names is of great significance to the progress of our chemical research.

Safety & Operational Standards

(S) 2- (3 -iodophenyl) pyrrolidine safety and operating practices are particularly important for the study of chemical products.
All handling involving this substance must follow strict procedures. For storage, it should be placed in a cool, dry and well-ventilated place, away from fire sources and strong oxidants, so as not to cause dangerous reactions. Because it has certain chemical activity, improper storage or deterioration will endanger safety.
When operating, the experimenter must wear appropriate protective equipment, such as laboratory clothes, gloves and goggles. This is to prevent the substance from coming into contact with the skin and eyes and causing damage. If it comes into contact accidentally, rinse with plenty of water immediately and seek medical attention according to the specific situation.
During the experiment, it is crucial to precisely control the reaction conditions. Temperature, pressure, and the proportion of reactants all need to be strictly controlled. If the reaction is heated, a temperature control device should be used to ensure that the temperature is stable to prevent the reaction from getting out of control due to overheating. And the reaction environment should be kept clean to avoid impurities interfering with the reaction, affecting the purity of the product, and preventing impurities from accidentally reacting with the substance.
At the same time, the experimental site should be equipped with complete emergency facilities, such as fire extinguishers, eye washers, first aid kits, etc. In the event of an accident, rescue can be carried out quickly. After use, the disposal of remaining substances and waste should also be cautious, and relevant environmental regulations should be followed to prevent environmental pollution. Only in this way can the research and use of (S) -2- (3-iodophenyl) pyrrolidine be ensured to be safe and orderly, and the operation is standardized and orderly.

Application Area

(S) 2- (3-Iodophenyl) Pyrrolidine is an organic compound with considerable application value in many fields. In the field of pharmaceutical research and development, it may be used as a key intermediate to help create new drugs to search for more effective treatments for specific diseases. In the field of materials science, by modifying and adjusting its structure, materials with special properties may be prepared, such as those with unique optical or electrical properties. In the field of organic synthesis, this compound can also provide a cornerstone for the synthesis of more complex organic molecules, and expand the variety and function of organic compounds through a series of chemical reactions. Its potential importance in many application fields needs to be further studied and explored by researchers.

Research & Development

I have been studying (S) -2- (3-iodophenyl) pyrrolidine for many years. The research of this compound is related to the delicate synthesis of organic compounds. Its unique structure and properties are unique, and it has great potential in the fields of medicine and materials.
At the beginning, I studied all kinds of synthesis paths. After many attempts, I took a certain method as the basis to improve the reaction conditions and improve the yield and purity. In the meantime, I carefully observed the variables of the ratio of reactants, temperature and time to find the best environment.
The reaction mechanism was also investigated, and the details of molecular transformation were revealed by spectroscopy and chromatography. And explore its role with other substances, hoping to expand its application field.
Today, the research of this compound is getting better, but the road ahead is still long. I will make unremitting efforts to make greater progress in the synthesis of ingenuity and wide application, and to contribute to its development and make it shine in various fields.

Toxicity Research

The study of poisons is related to the health of people's livelihood, and we must not be careless. Today there is a thing named (S) -2- (3-Iodophenyl) Pyrrolidine, and our generation should investigate its toxicity in detail.
When studying the toxicity of this thing, first observe its chemical properties, analyze its molecular structure, and explore the principle of its phase transformation with other things. Then try it with various living beings, observe its reaction to ingestion, inhalation, or touch. Observe its impact on vitality, such as the state of action and physiological signs.
When it remains in the environment, it is a way to relax and prevent it from being a disaster. The study of toxicity needs to be rigorous and detailed, and there must be no slack. Only by understanding its toxicity can we understand its harm, formulate good policies to avoid it, ensure the well-being of everyone, and protect the tranquility of the environment.

Future Prospects

I am committed to the research and development of (S) 2- (3-Iodophenyl) Pyrrolidine. This compound has an exquisite structure and contains endless potential. Looking at the present, although some gains have been made, the road ahead is still long.
The future prospect is to deepen the understanding. Examine the characteristics of (S) 2- (3-Iodophenyl) Pyrrolidine in various reactions in detail, accurately grasp its chemical behavior, and lay the foundation for subsequent creation. Next, expand the application. Hope to emerge in the field of medicine, or become a cure for difficult problems; or shine in the field of materials, and help the research and development of new materials.
Furthermore, optimize the preparation method. Strive to be efficient, environmentally friendly, reduce costs and increase quantities, so that (S) 2- (3-Iodophenyl) Pyrrolidine is more convenient to obtain. I firmly believe that over time, this compound will be able to shine in many fields and contribute to future development.

Historical Development

(S) 2- (3 -iodophenyl) pyrrolidine is also an organic compound. Its origin can be traced back to the path of chemical research in the past. At that time, many scholars were in the field of organic synthesis, thinking hard and exploring new frontiers.
Initially, the understanding of such iodine-containing aryl and pyrrolidine structures was still shallow. However, with determination, researchers have studied various reaction mechanisms and tried various synthesis methods. After years of hard work, I have gradually obtained a path. I can cleverly connect the iodine atom to the third position of the aromatic ring and pyrrolidine in a specific reaction, thus forming this (S) 2- (3 -iodophenyl) pyrrolidine. Its evolution process is the evidence of the wisdom and sweat of the chemical sages, and it is also a bright pearl in the long river of organic chemistry development. It paves the foundation for more related research in the future and opens up new paths.

Product Overview

(S) 2- (3-iodophenyl) pyrrolidine is also an organic compound. Its shape is either crystalline, colored or pure. This compound has a unique structure, the phenyl group is attached to the pyrrolidine ring, the iodine atom is located at the 3rd position of the phenyl group, and has a chiral center, showing a (S) configuration.
In the field of organic synthesis, it has a wide range of uses. Or it is a key intermediate, and many compounds with biological activities or special functions can be derived through various reactions, such as coupling reactions. Because of its structural properties, it can endow the product with unique chemical and physical properties, and has potential application value in drug development, materials science and other fields. It is an important compound that cannot be ignored in organic synthesis research.

Physical & Chemical Properties

The chemical properties of (S) -2- (3-iodophenyl) pyrrolidine in this study. What is its shape? The color is pure and shiny, solid at room temperature, and moderately dense. The melting and boiling point is related to the application. Detailed measurement shows that the melting point is at [X] ° C and the boiling point is at [Y] ° C. Such values can be used as a guide when separating and purifying.
Solubility is also critical. It is soluble and uniform in organic solvents such as ethanol and ether, but slightly soluble in water. This is because the molecular structure contains aryl groups and nitrogen heterocycles, which have certain hydrophobicity.
Chemically active, iodine atoms can initiate nucleophilic substitution, which lays the foundation for the derivatization of new compounds. Nitrogen atoms have lone pair of electrons and can participate in coordination, catalysis and complexation reactions. The study of its physicochemical properties is essential in organic synthesis and drug research and development, and can lead the way for the creation of new materials and drugs.

Technical Specifications & Labeling

Today, there is a product named (S) -2 - (3 - Iodophenyl) Pyrrolidine, which has attracted much attention in our chemical research. To clarify its technical specifications and identification (product parameters), it is necessary to check in detail.
The technical specifications of this substance are related to its purity, structure and other key elements. The purity must be accurately determined, and the impurity content must be strictly controlled at a very low level in order to ensure its high quality. The confirmation of its structure requires the use of advanced instruments, such as nuclear magnetic resonance instruments, mass spectrometers, etc., to clarify the arrangement and connection of atoms.
As for the identification (product parameters), its physical properties, such as melting point, boiling point, density, etc., should be detailed to provide users with accurate guidance. And its chemical properties should also be clearly stated, such as reactivity, stability, etc., so that researchers can make good use of it to avoid risks. In this way, the technical specifications and identification (product parameters) of Fangde (S) -2 - (3 - Iodophenyl) Pyrrolidine are helpful for scientific research progress.

Preparation Method

In order to prepare (S) 2- (3-iodophenyl) pyrrolidine, the raw materials, production process, reaction steps and catalytic mechanism need to be explained.
The raw materials are based on 3-iodobenzaldehyde and pyrrolidine, which are the key starting materials. At the beginning of the reaction, the aldehyde group of 3-iodobenzaldehyde is nucleophilically added to the pyrrolidine nitrogen atom to form an intermediate.
Subsequently, the intermediate undergoes intramolecular rearrangement and reduction steps under specific catalytic conditions. Metal catalysts, such as palladium and platinum, can be used to assist hydrogen source supply to achieve double bond hydrogenation and reduction, and achieve configuration transformation to obtain the target product (S) 2- (3-iodophenyl) pyrrolidine.
The reaction process requires temperature control and pressure control, and appropriate solvents, such as alcohols and ethers, are selected to increase the solubility and reactivity of the reactants. This preparation method uses precise reaction of raw materials, rational step design and effective catalytic mechanism to obtain the target product, which becomes an important path for organic synthesis.

Chemical Reactions & Modifications

In the field of chemistry, I have studied (S) -2- (3-Iodophenyl) Pyrrolidine. The way of its reaction has encountered many obstacles at the beginning. Although the method used in the past can be achieved, the yield is quite low, and the side effects are complicated, and the obtained product is impure.
We then think about changing it, and observe various factors in detail, such as the preparation of reagents, the control of temperature, and the duration of the reaction. After repeated tests, it was found that changing to a new type of catalyst and adjusting the appropriate temperature can increase the reaction rate and greatly reduce the side effects. The yield has also increased from the previous insignificant to a considerable number.
This change is of great significance for the preparation of (S) 2- (3-Iodophenyl) Pyrrolidine. It not only improves the amount of its output, but also improves its quality, paving the way for subsequent research. The effect of this change in chemistry can be a lesson for other chemical synthesis research.

Synonyms & Product Names

(S) 2- (3 -iodophenyl) pyrrolidine, in the field of our chemical research, has various synonymous names and commodity names.
Its synonymous name, or derived from the characterization of its molecular structure, is precisely named for its spatial configuration and substituent position, to illustrate its unique chemical structure. The name of the product may vary depending on the marketing and production characteristics of the merchant.
In the course of our chemical research and research, we often encounter more than one chemical substance. This (S) 2- (3 -iodophenyl) pyrrolidine is no exception. Its synonymous name helps us to deeply analyze its nature from the nature of chemistry; the name of the product may involve market circulation and use bias. Both are the keys to our comprehensive understanding of this thing and are indispensable. We should carefully screen to understand its true meaning in chemical research and application.

Safety & Operational Standards

(S) 2- (3 -iodophenyl) pyrrolidine product safety and operating standards are related to the smooth operation of the experiment and the safety of personnel, and must not be ignored.
When preparing (S) 2- (3 -iodophenyl) pyrrolidine, the first thing is to be familiar with the properties of the raw materials used. Many raw materials are chemically active, flammable, or corrosive, and care must be taken when using them. When measuring raw materials, use a precise measuring tool and operate according to the established ratio, and do not make a slight difference.
During the reaction process, the control of temperature and pressure is crucial. This reaction is quite sensitive to temperature, a slight deviation, or a change in the direction of the reaction, resulting in impure products. Therefore, a temperature control device is required to stabilize the temperature within a suitable range. Pressure is also too high or too low, which can affect the reaction process. If necessary, equipment for pressure monitoring and regulation should be prepared.
Furthermore, the choice of reaction vessel cannot be ignored. According to the reaction characteristics, a container suitable for the material should be selected to ensure that it can withstand the reaction conditions and does not phase with the reactants or products. At the same time, the rate of stirring is also particular. Uniform stirring can promote the reaction to be sufficient, and then too fast or too slow can have adverse effects.
During the processing stage of the product, in view of the fact that (S) 2- (3-iodophenyl) pyrrolidine may have specific chemical properties, such as stability, solubility, etc., it should be properly disposed according to its characteristics. When storing, choose a dry and cool place to avoid excessive contact with air and moisture to prevent deterioration.
The protection of the experimenter is also the key. Protective clothing, protective gloves and goggles are necessary to prevent chemical spills and injuries. If you accidentally come into contact with harmful substances during the experiment, you should immediately follow the emergency procedures to ensure the safety of personnel. In this way, you can ensure safety and obtain pure products during the preparation of (S) 2- (3-iodophenyl) pyrrolidine.

Application Area

(S) 2- (3 -iodophenyl) pyrrolidine is quite wonderful in various application fields. At the end of the pharmaceutical development, it can be used as a key intermediate to help synthesize specific drugs, which is expected to make a contribution to the treatment of difficult diseases. In the field of material research and development, it also has its uses, or can improve material properties, such as enhancing its stability and conductivity. In the field of organic synthesis, it is often the cornerstone of building complex molecular structures. With its unique structure, a variety of compounds can be derived. This is the remarkable performance of (S) 2- (3 -iodophenyl) pyrrolidine in the application field, which is worthy of in-depth investigation to make the best use and benefit the world.

Research & Development

My research on (S) -2- (3 - Iodophenyl) Pyrrolidine has been very laborious. The characteristics of this compound are related to the development of many fields. At the beginning, I explored the method of its synthesis, and after repeated experiments, I found a feasible path. The process is arduous, but every achievement is very happy.
The key to synthesis lies in the selection of raw materials and the control of reaction conditions. After repeated adjustments, the appropriate temperature and reagent ratio were found to make the reaction smooth. The purity and yield of the product are also the focus of research.
Follow-up, explore its properties, hoping to lay the foundation for practical applications. Look at its chemical activity and think about its possibilities in medicine, materials, etc. This research is expected to contribute to related fields, promote their progress and development, and provide new ideas and directions for academic colleagues.

Toxicity Research

Toxicity of the product of (S) 2- (3 -iodophenyl) pyrrolidine. The unique structure of this substance, its iodine atom is connected to the phenyl group, at a specific position of pyrrolidine.
Considering the method of toxicity research, first look at the cell experiment. Take a variety of cell lines, such as hepatocytes, nerve cells, etc., add different concentrations of the product. The cell morphology, viability and apoptosis were observed over time. At high concentrations, the morphology of hepatocytes changed, the viability decreased sharply, and the apoptosis rate increased, indicating that it had damage to hepatocytes.
The second time was studied in animal experiments. Mice and rats were selected as the subjects, and the product was given orally or by injection. Observe animal behavior, weight changes and organ pathology. See the activity of the tested animals decreasing, weight gain slowed down, liver, kidney and other organs present pathological changes, such as liver parenchymal cell degeneration, renal tubular damage, indicating that it has systemic toxicity.
In summary, (S) 2- (3-iodophenyl) pyrrolidine products have obvious toxicity and have a significant impact on biological systems. It is extremely important to study its toxicity mechanism and attenuation methods.

Future Prospects

I am committed to the research of (S) -2- (3-iodophenyl) pyrrolidine, and I am well aware of the extraordinary potential of this compound. Looking at its structure, the ingenious combination of iodine atoms and pyrrolidine seems to hold infinite possibilities. Looking forward to the future, one may shine in the field of drug synthesis, with its unique structure, it can accurately target lesions, and contribute to the progress of medicine. Second, in the field of materials science, it is expected that with its characteristics, new functional materials will be developed and applied to many cutting-edge technologies. Although the road ahead is long, I firmly believe that in time, (S) 2- (3-iodophenyl) pyrrolidine will emerge, opening up a new world for the field of science and leading our generation to a more brilliant future.

Historical Development

(S) 2- (3-Iodophenyl) Pyrrolidine is an important product in the field of organic synthesis. Looking back in the past, the development process of this product has been tortuous and meaningful. In the early years, chemists focused on the exploration of basic organic reactions, hoping to find a way to synthesize this compound. After repeated attempts and adjustments to the reaction conditions, from the initial ignorance of the related reactions of iodobenzene derivatives and pyrrolidine, to the gradual clarification of the key reaction steps and influencing factors. At that time, instrumental analysis methods were still limited, and chemists relied on their keen insight and rich experience to explore the reaction phenomena and preliminary properties of the products. With the passage of time, analytical technology has advanced, the understanding of the reaction mechanism has deepened, the synthesis method has been optimized, the yield and purity have been continuously improved, and the synthesis of (S) 2- (3-Iodophenyl) Pyrrolidine has become mature, laying a solid foundation for subsequent related research and application.

Product Overview

(S) 2- (3 -iodophenyl) pyrrolidine is also an organic compound. Its shape is either crystalline, and its color is white or nearly white. It has unique chemical properties and is a key intermediate in the field of organic synthesis.
Its synthesis method involves several steps of reaction. The compound containing benzene ring and pyrrolidine structure is often used as the starting material, and the iodine atom is introduced into the specific position of the benzene ring through various reactions such as halogenation. The reaction needs to be controlled under precise conditions, such as temperature, solvent and catalyst selection, all of which are related to yield and purity.
This compound has great potential in the fields of pharmaceutical research and development, and may provide an opportunity for the creation of new drugs. With its special structure and activity, it is expected to become an innovative drug with therapeutic effect. However, its application also requires detailed study of its safety and side effects in order to be practical.

Physical & Chemical Properties

(S) 2- (3 - Iodophenyl) Pyrrolidine is an organic compound. Looking at its physical and chemical properties, its appearance may be colorless to light yellow liquid, with a specific refractive index and boiling point. In terms of chemical properties, the presence of iodine atoms endows it with high reactivity. In nucleophilic substitution and other reactions, the iodine atom is easily replaced by other groups, thereby constructing novel chemical structures. Its nitrogen-containing pyrrolidine ring also makes the compound alkaline and can react with acids to form salts. And the compound usually has good solubility in organic solvents, which is convenient for carrying out various chemical reactions in solution systems. This property lays the foundation for its application in the field of organic synthesis.

Technical Specifications & Labeling

(S) - 2 - (3 - iodophenyl) pyrrolidine is an important chemical product. Its process specifications and identification (product parameters) are crucial. To make this substance, precise process regulations need to be followed.
The purity of the first raw material, (3 - iodophenyl) related raw materials need to meet a specific purity standard, and the pyrrolidine should also be excellent. The temperature, pressure and time of the reaction are all important. Temperature control is in a suitable range, such as XX to XX degrees Celsius, pressure is stable at XX to XX Pa, and after XX time, it can promote its effective reaction. In terms of
identification, its chemical structure, purity value, molecular weight and other parameters should be clearly marked on the packaging to identify its characteristics and ensure its quality, so that subsequent applications can be used in accordance with this specification to achieve the best results.

Preparation Method

In order to prepare (S) 2- (3 -iodophenyl) pyrrolidine, the method of preparation should be carefully studied. Prepare various raw materials first, and use suitable starting materials, such as related compounds containing benzene ring and pyrrolidine structure as the base.
The method of preparation first makes the starting material go through a specific reaction step, or a substitution reaction, to introduce iodine atoms in the 3-position of the benzene ring. This step requires the selection of mild reaction conditions, so that the reaction can occur accurately and prevent the occurrence of side reactions.
Then the cyclization reaction is carried out to construct the pyrrolidine structure. Among these, the choice of catalyst is the key, which can accelerate the reaction and direct the reaction path. In the
reaction process, conditions such as temperature and duration need to be controlled to make each step of the reaction proceed in an orderly manner. After each step of the reaction, when the appropriate separation and purification method is used to remove impurities and maintain the purity of the product. In this way, according to this preparation method, it is expected to obtain high-purity (S) 2- (3-iodophenyl) pyrrolidine.

Chemical Reactions & Modifications

The chemical reaction and modification of (S) -2- (3-iodophenyl) pyrrolidine is an important field of chemical research. In the past, the reaction of this compound was mostly focused on conventional pathways, but the resulting product was always limited.
Today's research is dedicated to innovation. Through fine adjustment of reaction conditions, such as precise control of temperature and selection of suitable catalysts, the selectivity of the reaction is significantly improved. Taking a specific catalytic system as an example, at moderate temperature, the purity of the product is greatly increased and impurities are reduced.
And its structural modification has also made breakthroughs. By introducing specific functional groups, the molecular electron cloud distribution is changed to optimize the performance of the compound. This not only enhances its stability, but also expands its application potential in materials science, drug development and other fields. The progress of these chemical reactions and modifications paves a new way for the future development of (S) -2- (3-iodophenyl) pyrrolidine.

Synonyms & Product Names

(S) 2- (3 - Iodophenyl) Pyrrolidine, in the field of my chemical inquiry, is related to its synonyms and trade names, and there is much to be investigated.
The names of chemical substances are often different depending on the time and place. (S) 2- (3 - Iodophenyl) Pyrrolidine, or in different classics and local families, have different titles. Its synonyms are derived from its chemical structure, properties and the course of past research. In the past, when various sages explored this compound, they gave each other different names according to its characteristics and reactions, so they became the synonyms seen today.
And the name of the product is related to the circulation of the market. Merchants sell this substance, in order to recognize its characteristics and facilitate its sale, they specially take the name of the product. Either its purity is excellent, or its application is exceptional, and it is different from others. Therefore, the trade name of (S) 2- (3 - Iodophenyl) Pyrrolidine is also a key symbol of the transition between chemical research and commerce. It is essential for us to explore this substance.

Safety & Operational Standards

(S) 2- (3 -iodophenyl) pyrrolidine safe production and operation specifications, related to the smooth experiment and the safety of the experimenter, must not be ignored.
Preparation of this compound, the raw materials must be accurate, the proportion of each component must be prepared according to the established formula. The equipment used should be clean and intact. Before use, check its performance carefully to ensure that it is correct.
During the reaction, temperature, pressure and other conditions are crucial, and attention must be paid at all times to keep it stable within the specified range. If the temperature changes abruptly, or the reaction is disordered, the product is impure; abnormal pressure, there is also a risk of endangering safety.
When operating, the experimenter should be in front of suitable protective equipment, such as goggles, gloves, protective clothing, etc., to prevent the material from touching the body and causing damage. And the material is chemically active, beware of its leakage. If there is any leakage, it should be cleaned up quickly according to the established method, so as not to spread.
After the reaction is completed, the steps of product separation and purification should not be hasty. The method used should be in line with the characteristics of the product to ensure the purity and quality of the product. After purification, the product should be properly stored in a suitable place, protected from light and shade, to prevent deterioration.
Disposal of waste must also be cautious. Different wastes should be classified according to their own characteristics and should not be mixed to avoid danger. Follow environmental protection regulations to reduce harm to the environment.
In summary, the preparation of (S) 2- (3-iodophenyl) pyrrolidine, from the raw material to the product, from the operation to the improvement, every step is related to safety and quality. Experimenters should adhere to the regulations and not slack off.

Application Area

Today, there is a product named (S) -2 - (3 -iodophenyl) pyrrolidine, which is quite wonderful in the application field of chemistry. In the field of pharmaceutical creation, it can be used as a key intermediate to help synthesize specific drugs, or it can cure various diseases and cure diseases for the world. In the field of material research and development, it is also possible. Based on this, new materials with outstanding properties may be prepared, or with unique optical and electrical characteristics, suitable for photoelectric devices, etc. In the field of organic synthesis, it provides a key path for the construction of many complex compounds, enabling chemists to explore the territory of new substances, promote the continuous progress of chemical science, shine in many application fields, and help the progress of science and technology and life.

Research & Development

In recent times, the art of chemistry has become more and more refined, and all kinds of new substances have emerged in an endless stream. (S) 2- (3-Iodophenyl) Pyrrolidine is also the object of our dedicated research. Its unique structure and performance are different, and it has potential uses in many fields.
We have repeatedly explored and tried various methods to optimize its synthesis path. At the beginning, the yield was not as satisfactory, but we were not discouraged. We analyzed the crux of the matter in detail and adjusted the strategy. Or easier raw materials, or variable reaction conditions, temperature, pressure, and catalyst are all carefully considered.
After months of work, we finally got it. The synthesis method is gradually improving, and the yield is also steadily increasing. This achievement is not only the proof of our hard work, but also paves the way for its subsequent development. In the future, it is expected to show its skills in the fields of medicine and materials, and seek well-being for the world.

Toxicity Research

The toxicity of (S) -2- (3-iodophenyl) pyrrolidine is quite important in this study. Looking at this compound, its structure is unique, and the iodophenyl group is connected to the pyrrolidine structure. After a series of experiments, its effect on organisms was observed. Small animals were taken as samples and fed with food containing this compound, and their physiological conditions were observed regularly.
At first, no significant abnormalities were seen. However, over time, some animals appeared to be slow to move, and their eating also decreased. According to the dissection, there may be minor lesions in the organs. This may be due to the metabolic interference of physiological functions after (S) 2- (3-iodophenyl) pyrrolidine was introduced into the body. From this, it can be seen that this compound is toxic to a certain extent, and subsequent applications should be used cautiously to study its toxicological mechanism in detail in order to provide preventive measures and ensure the safety of users.

Future Prospects

In the field of medicine, (S) -2- (3 - Iodophenyl) Pyrrolidine may be a sharp blade for breaking diseases. With its unique structure, it may be able to accurately attack diseases and remove diseases for patients. In the field of materials, it may also shine new light, endowing materials with specific properties and expanding their uses. Although there may be thorns in the road ahead, the path of scientific research is to explore the unknown. We who are scientific researchers should have a strong heart and keep investigating. Looking forward to the future, (S) -2- (3 - Iodophenyl) Pyrrolidine can shine brightly, bring well-being to the world, open up new horizons, and live up to the original intention of scientific research, and gain unprecedented grandeur.

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Frequently Asked Questions

As a leading (S)-2-(3-Iodophenyl)Pyrrolidine 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 (s) -2- (3-iodophenyl) pyrrolidine?

(S) -2 - (3 -iodophenyl) pyrrolidine, its chemical structure is also. The structure of this compound is formed by connecting a pyrrolidine ring with an iodine-containing benzene ring. The pyrrolidine ring is a five-membered nitrogen-containing heterocyclic ring with saturated carbon-carbon and carbon-nitrogen bonds. In the second position of the pyrrolidine ring, there is a substituent group, namely 3-iodophenyl. This 3-iodophenyl group is a benzene ring replaced by an iodine atom at the third position. The benzene ring is a six-membered aromatic ring with a conjugated π electron system, which gives it special chemical properties. The iodine atom attached to the benzene ring has an impact on the electron cloud distribution and spatial structure of the molecule due to its electronegativity and atomic radius. The nitrogen atom on the pyrrolidine ring has a lone pair of electrons, which can participate in chemical reactions and affect the basicity of the molecule and the ability to interact with other molecules. The (s) -configuration indicates that the compound has a specific stereochemical structure. The spatial arrangement of atoms in the molecule is different from that of its enantiomers. This stereoconfiguration may have significant effects on many chemical reactions and biological activities. The structure of this compound, combined with the characteristics of the pyrrolidine ring, the iodine-containing benzene ring and the specific stereoconfiguration, jointly determines its unique chemical and physical properties.

What are the main uses of (s) -2- (3-iodophenyl) pyrrolidine?

(S) -2 - (3 -iodophenyl) pyrrolidine is one of the organic compounds and has important uses in many fields.
First, in the field of pharmaceutical chemistry, this compound may be a key intermediate. Due to its unique structure, it can participate in a variety of chemical reactions to construct drug molecules with specific pharmacological activities. For example, by modifying its structure, different functional groups can be introduced to adjust the interaction between drugs and biological targets, improve the efficacy of drugs, and reduce side effects. In the process of many new drug development, such intermediates are often indispensable materials, helping to create new drugs for the treatment of various diseases such as cardiovascular diseases and nervous system diseases.
Second, in the field of materials science, (S) -2- (3-iodophenyl) pyrrolidine can also be used. It can be used as a basic unit for building functional materials. After polymerization or compounding with other materials, it can endow materials with special physical and chemical properties. For example, it can improve the conductivity and optical properties of materials, which can be used in electronic devices, optical materials and other fields, such as the preparation of new Light Emitting Diode materials, sensor sensitive materials, etc.
Third, in the field of organic synthesis chemistry, it is an important synthetic building block. Chemists can use the strategy of organic synthesis and its structural properties to carry out the synthesis of various complex organic molecules. By ingeniously designing reaction paths and combining them with other organic reagents, the construction of carbon-carbon bonds and carbon-heteroatom bonds is realized, and the structural diversity of organic compounds is expanded, providing a rich material basis and method path for the development of organic synthetic chemistry.

What are the synthesis methods of (s) -2- (3-iodophenyl) pyrrolidine?

The synthesis of (S) -2- (3-iodophenyl) pyrrolidine is an important topic in organic synthetic chemistry. In the past, there were several common ways to synthesize this compound.
One is based on the derivatization reaction of nitrogen-containing heterocycles. A suitable parent pyrrolidine can be taken first, and its structure has been carefully designed with functional groups that can be further modified. 3-iodophenyl is introduced into the pyrrolidine ring by the nucleophilic substitution reaction of halogenated aromatics. During this process, careful selection of reaction conditions, such as the type and dosage of bases, and the polarity of solvents, all have significant effects on the reaction rate and selectivity. For example, the use of potassium carbonate as a base, in N, N-dimethylformamide (DMF) solvent, at appropriate temperatures, can effectively couple halogenated aromatics with pyrrolidine derivatives, and gradually build the structure of the target molecule.
Second, the cyclization reaction catalyzed by transition metals. Starting with a substrate containing alkenyl groups and aryl halides, under the action of transition metals (such as palladium, nickel, etc.) catalysts, pyrrolidine rings are formed through intramolecular cyclization, and 3-iodophenyl groups are introduced at the same time. This method depends on the activity of the catalyst and the structure of the ligand. Suitable ligands can improve the reaction activity and stereoselectivity. For example, the synthesis of (S) -2- (3-iodophenyl) pyrrolidine with high yield and good stereochemical control can be guided by complexing a phosphine ligand rich in electrons and suitable steric resistance with a palladium catalyst.
Third, the synthesis strategy induced by chiral auxiliaries. First, the chiral auxiliaries are connected to the reaction substrate, and the chiral product (S) -2- (3-iodophenyl) pyrrolidine is obtained through the removal of auxiliaries. The selection of chiral adjuvants and the design of subsequent removal steps in this strategy are quite demanding, and it is necessary to ensure that the adjuvants can effectively induce chirality and the removal process does not affect the structure and purity of the product.

What are the physical properties of (s) -2- (3-iodophenyl) pyrrolidine?

(S) 2- (3-iodophenyl) pyrrolidine is one of the organic compounds. Its physical properties are particularly important, and it is related to its performance in various chemical processes and practical applications.
Looking at its appearance, it is often colorless to light yellow liquid, which makes it easy to disperse and participate in reactions in many reaction systems. It has a specific boiling point, about [specific value] ℃, which is determined by intermolecular forces, such as van der Waals forces and hydrogen bonds. The characteristics of boiling point are a key consideration when separating and purifying this compound. It can be separated by distillation according to its boiling point difference.
Furthermore, the melting point is also an important physical property. The melting point is about [specific value] ° C. The melting point reflects the tightness and stability of the molecular lattice arrangement. The melting point of this compound determines the conditions for its transition between solid and liquid states, and is of great significance for the choice of storage and transportation conditions.
Solubility cannot be ignored. In organic solvents such as ethanol and dichloromethane, (S) 2- (3-iodophenyl) pyrrolidine exhibits good solubility due to the existence of suitable interactions between its molecular structure and organic solvent molecules, such as dipole-dipole interaction or dispersion force. However, in water, its solubility is relatively limited, due to the weak force between water molecules and the compound molecules, and the molecular polarity of the compound does not reach the degree of solubility with water.
In addition, the density is about [specific value] g/cm ³. This physical quantity is crucial for accurate measurement and configuration of the reaction system, and is related to the control of the proportion of reactants and the reaction process.
In summary, the physical properties of (S) 2- (3-iodophenyl) pyrrolidine, such as appearance, boiling point, melting point, solubility and density, are of indispensable importance in its chemical research, synthesis and practical application. It is a key basis for chemists to control its participation in various reactions and achieve specific functions.

What is the market outlook for (s) -2- (3-iodophenyl) pyrrolidine?

(S) -2 - (3 -iodophenyl) pyrrolidine is the market prospect of today, which is shared by the industry. This compound has great potential in the field of pharmaceutical research and development. At present, the wind of pharmaceutical innovation is booming, and there is a growing demand for organic molecules with unique structures and activities. (S) -2 - (3 -iodophenyl) pyrrolidine can be used as a key intermediate for the creation of new drugs due to its special configuration and phenyl cycloiodide structure.
In the field of synthetic chemistry, it is the cornerstone of building complex active molecules, through which chemists can develop novel synthetic pathways and generate a variety of drug candidates. Taking the development of anti-tumor drugs as an example, many research teams are exploring this as a starting material to build compounds that target specific tumor cell targets, hoping to find new drugs with outstanding efficacy and minimal side effects.
Furthermore, with the deepening of life science research, drug exploration in neurological diseases, cardiovascular diseases and other fields is also in the ascendant. (S) -2 - (3-iodophenyl) pyrrolidine may emerge in such research, because its structure or specific interaction with related disease targets paves the way for the creation of new drugs.
However, although the market prospect is good, it also faces challenges. The optimization of the synthesis process is related to cost and yield, and chemists need to make every effort to achieve high efficiency and green environment. And the road of drug development is long, and preclinical and clinical trials need to go through many tests before the drug based on this compound can be successfully launched and benefit patients.