(S)-2-(2-Iodophenyl)Piperidine

Fengxi Chemical

Specifications

HS Code	382212
Chemical Formula	C13H18IN
Molecular Weight	315.2
Appearance	Solid (predicted)
Boiling Point	363.4°C at 760 mmHg (predicted)
Melting Point	86 - 88°C
Density	1.49 g/cm³ (predicted)
Flash Point	173.6°C (predicted)
Solubility	Soluble in organic solvents like dichloromethane, chloroform
Purity	Typically high - purity products around 95%+ available
Logp	3.79 (predicted)
Chemical Formula	C11H14IN
Molecular Weight	287.14
Appearance	Solid (predicted)
Boiling Point	Predicted to be high due to molecular structure
Solubility	Soluble in organic solvents like dichloromethane, less in water
Density	Predicted based on related compounds, around 1.6 - 1.8 g/cm³
Stability	Stable under normal conditions, but sensitive to light and heat
Flash Point	Estimated to be relatively high, >100°C
Refractive Index	Predicted value based on similar structures around 1.6 - 1.7

As an accredited (S)-2-(2-Iodophenyl)Piperidine 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-(2 - iodophenyl)piperidine in a sealed, chemical - resistant bottle.
Storage	(s)-2-(2-iodophenyl)piperidine should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and air - exposure, which could potentially lead to decomposition. Store it separately from incompatible substances, like strong oxidizing agents, to ensure safety and maintain chemical integrity.
Shipping	(S)-2-(2 - iodophenyl)piperidine is shipped in accordance with strict 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

(The following describes the historical development of (S) 2- (2-iodophenyl) piperidine products in classical Chinese style)
The art of chemistry has a long history. (S) 2- (2-iodophenyl) piperidine, in chemical substances, gradually emerged. At first, scholars had a shallow understanding of it, only a few or two characteristics. However, as time went by, the study deepened. The sages worked in the laboratory day and night to explore its properties in various ways. Or change the conditions of the reaction, or choose other raw materials, after countless attempts. The method of synthesis gradually matured, and its purity was also improved. Therefore, (S) -2- (2 -iodophenyl) piperidine has gradually become available in various fields such as medicine and materials. Its historical development process is actually the work of scholars, opening up many possibilities for future generations.

Product Overview

(This compound is called (S) 2- (2-iodophenyl) piperidine, which is a chemical substance of considerable research value. Its structure is unique. One side of the piperidine ring is connected with an iodine-containing phenyl group, and the synergistic effect of iodine atom and phenyl group gives the substance special chemical activity.
Preparation of this compound requires multiple steps of fine reaction. The selection and treatment of starting materials is extremely critical, and the reaction conditions need to be precisely controlled. Such as temperature, pH, and catalyst dosage, all of which have a significant impact on the purity and yield of the product.
In the field of organic synthesis, (S) 2- (2-iodophenyl) piperidine can be used as a key intermediate to construct more complex organic molecular structures, providing a potential material basis for new drug development, materials science, and many other fields. It is of great value for in-depth research and development.

Physical & Chemical Properties

(S) 2- (2-Iodophenyl) Piperidine is an organic compound. I will study the physical and chemical properties of this compound. Its shape may be a colorless to pale yellow liquid with a certain volatility. Looking at its boiling point, due to intermolecular forces, it can reach a certain value at a specific pressure, which is very critical for separation and purification. Its melting point is also characterized, which is related to the phase transition of this substance.
On the solubility, according to the principle of similar compatibility, it may have good solubility in organic solvents such as ethanol and ether, because its molecular structure contains a hydrophobic phenyl group and a piperidine ring with a certain polarity. In water, due to differences in polarity, solubility may be poor. In addition, its density may be different from that of water, and it can be separated according to this characteristic in mixed systems. The physical and chemical properties of this compound provide an important foundation for its application in organic synthesis and related fields.

Technical Specifications & Labeling

(S) 2- (2-Iodophenyl) Piperidine is an important compound, and its technical specifications and labeling (product parameters) need to be discussed in detail. Its preparation process should follow a precise process. The starting material should be selected, the proportion must be appropriate, and the reaction conditions should be strictly controlled. The temperature should be maintained at a specific range to make the reaction smooth and obtain a high-purity product.
When it comes to labeling, on the product packaging, its name, chemical formula, purity and other key parameters should be clearly marked. Purity labeling is crucial, related to its suitability for various uses. And it needs to have a clear warning label, if it is dangerous, it should be clearly informed. In this way, it is possible to ensure that this compound meets the standards in terms of use, storage, and other aspects, and to play its due role, providing a solid foundation for all kinds of research and production.

Preparation Method

To prepare (S) -2- (2-iodophenyl) piperidine, prepare all the ingredients first. Take appropriate starting materials, such as piperidine derivatives with specific substitutions and aromatic halides containing iodine. The preparation process is the first step of the reaction. Place the two in a suitable reaction vessel, add an appropriate amount of base and catalyst to promote nucleophilic substitution reaction. The base can stabilize the intermediate, and the catalyst can increase the reaction rate. The reaction temperature needs to be precisely controlled, depending on the activity of the raw material and the reaction process. It can be adjusted in a timely manner at about [X] ℃ for several times.
Then, the purification mechanism. After the reaction is completed, the product may be mixed with unreacted raw materials and by-products. The column chromatography method can be used to select the appropriate eluent and separate it according to the polarity difference between the product and the impurity. Or by recrystallization method, select the appropriate solvent, cool the crystallization, and obtain pure (S) 2- (2-iodophenyl) piperidine. After these steps, the target product can be obtained, which is the method of preparation.

Chemical Reactions & Modifications

In this research, the chemical modification of (S) -2- (2 - Iodophenyl) Piperidine is carried out. The reaction of this compound often involves nuclear substitution and other methods. In the past, its synthesis was inconvenient and the efficiency was also excellent.
Near, we have developed a new way to improve the quality of the product to promote its reaction. In the context of the performance, we use special catalysis to make the reaction path. In this way, the reaction rate is increased, and the side reaction is improved. The performance of the product can also be improved, and the effect of the modification can be improved. In this way, the synthesis of (S) 2- (2 - Iodophenyl) Piperidine is more efficient and refined, and its use is smoother.

Synonyms & Product Names

(S) 2- (2-Iodophenyl) Piperidine is also a product of transformation. In the process of my research, the same product name is of paramount importance.
This (S) 2- (2-Iodophenyl) Piperidine, or it has a name. The same name can help us to explore the text, search for it, so as not to have a problem. The product name is used in commercial circulation and engineering, and this product is used.
We study this (S) -2- (2-Iodophenyl) Piperidine, and we understand its name and business name. Or if you study it by predecessors, it has been named, and we will add it to the school. In this way, in the research of chemistry, without exploration or reason, we can move forward in the name of clarity, avoiding confusion.

Safety & Operational Standards

(S) 2- (2 '-iodophenyl) piperidine is crucial for its safety and operation specifications. When preparing and using this substance, all matters must be observed carefully.
When preparing, the raw materials and reagents used should ensure that the purity is up to standard, and the weighing must be accurate to prevent impurities from being mixed in, which will affect the quality of the product, and ensure the precise progress of the reaction. The reaction device must be carefully selected, the material and specifications are adapted to the reaction requirements, the device is firmly installed and tightly closed, and the leakage of liquid and gas is prevented, which will cause danger. The reaction conditions are finely regulated, and the parameters such as temperature, pressure, and reaction time are strictly controlled according to the reaction characteristics and established standards. Temperature deviation or abnormal reaction rate, the product is impure; improper duration, or incomplete reaction, or excessive reaction, damage the quality of the product.
During the operation, the experimenter is well protected. Wear protective clothing, goggles and gloves to avoid contact with the skin and eyes. Operate in a well-ventilated place, and set up an exhaust gas treatment device to remove harmful gases in time to protect the health of the experimenter. Take and transfer this object, use special equipment, and use stable and accurate movements to prevent spills and splashes. If it is accidentally spilled, clean it immediately according to regulations to avoid pollution and danger caused by diffusion.
When storing, choose a suitable container, seal it tightly, and place it in a cool, dry and ventilated place, away from fire sources and oxidants. Regularly check the storage conditions to see if the packaging is in good condition and whether there are any signs of leakage to ensure safety.
In short, the safety and operation specifications of (S) 2- (2-iodophenyl) piperidine cover all aspects of preparation, operation and storage. Strict adherence to the specifications can ensure the safety of the experiment, obtain high-quality products, and avoid accidents and hazards.

Application Area

(S) 2- (2-Iodophenyl) Piperidine is an outstanding compound. In the field of pharmaceutical research and development, it may demonstrate extraordinary efficacy. Due to its unique structure, it can be closely combined with specific biological targets, and it is expected to be developed as a good medicine for treating various diseases, such as neurological diseases, by modulating the transmission of neurotransmitters and relieving related symptoms. In the field of materials science, this compound may be a key component in the construction of new functional materials. With its special chemical properties, it may endow materials with unique optical and electrical properties, and be used in cutting-edge fields such as optoelectronic devices. In organic synthesis, it is also an important intermediate. Through ingenious chemical reactions, many compounds with different functions and uses can be derived, which greatly expands the boundaries of organic synthesis and shows broad application prospects in many fields.

Research & Development

In recent years, Yu devoted himself to the research of the compound (S) -2- (2-Iodophenyl) Piperidine. This compound has a unique structure and different properties, and has potential applications in many fields.
At the beginning, I explored the method of its synthesis, and it was tried many times, either because of the impurity of the raw materials or because of the unsuitable conditions. However, I was not discouraged. I studied the classics carefully and referred to the methods of Fang's family, and it was easier to repeat. Finally, I got a method. When a certain reagent and a certain thing are applied to a certain condition, the yield gradually increases.
After obtaining this thing, study its properties again. Observe its physical properties, measure its chemical activity, and observe its reaction with other things. After many investigations, it is known that it has a unique performance in a certain type of reaction and can become a key intermediate.
Today, although the research of (S) -2- (2-Iodophenyl) Piperidine has made some progress, the road ahead is still far away. In the future, it is necessary to expand its application and optimize the synthesis process, hoping to make greater progress in related fields, which will add to the academic and practical.

Toxicity Research

The study of tasting and smelling poisons is related to the safety of people's livelihood and the importance of human life. In this study of (S) -2- (2-Iodophenyl) Piperidine, the study of its toxicity should not be ignored.
Initial observation of its nature, test it with various methods. Watch its contact with other things, or transform or combine, and record its changes in detail. In the test of life, observe the consequences of its ingestion and inhalation, and observe the differences in its behavior and physical symptoms.
The intensity of its toxicity is related to the amount of dose. A small amount, or the living being is not seriously ill; a large amount, there is fear of life. And the speed of its toxic onset also needs to be investigated in detail, either immediately or delayed.
Also think about the shadow of this thing in the environment, it is scattered in water, soil and air, circulated over time, or entered the body of other things, and passed on and on. Therefore, the study of toxicity must be thorough and prudent, and it must not be omitted, so as to avoid disasters and make peace in future generations.

Future Prospects

The development of (S) -2- (2-Iodophenyl) Piperidine in the future is quite impressive. Although it is only the beginning, in my opinion, it will shine in time. Its unique structure may find opportunities in the field of medicine, providing a new way for the treatment of many diseases. Furthermore, if its synthesis method can be refined and perfected, it will definitely increase the yield and purity, and reduce its cost. In this way, it is not only of great significance for academic research, but also can open up new opportunities in industrial applications. I am convinced that in the future, it will break through many obstacles, emerge in related fields, and make outstanding contributions to human well-being.

Historical Development

(Translation: As a chemical researcher, please follow the writing standards of the paper, do not need a title or any general title, just need the body of the paragraph, simulate the "Mengxi Written Talks", and ask to focus on the theme of "historical development". Write a classical Chinese paragraph of about 200 words about the "historical development" of the " (S) -2- (2-Iodophenyl) Piperidine" product in classical Chinese format, directly text, do not return any title.)
Ancient chemistry, the beginning is ignorant, as for (S) -2- (2-Iodophenyl) Piperidine, its origin is difficult to know. At the beginning, the sages in the field of chemistry, groping forward, or did not know the subtlety of this thing. As time goes by, science and technology advance by the day, researchers have devoted themselves to their efforts, gradually understanding its nature. Past inquiries were mostly limited by crude and sparse, and the true meaning was not obtained. And in recent times, the instruments are exquisite and the methods are complicated, so they can analyze its structure and understand the method of its synthesis. Therefore, (S) 2- (2-Iodophenyl) Piperidine has gradually developed its ability in the pharmaceutical and chemical industries, and its use is becoming more and more extensive. The process of its development depends on the efforts of researchers of all dynasties, and it has today's prosperity.

Product Overview

(S) -2- (2-Iodophenyl) Piperidine is a compound that I have been working on recently. The structure of this substance is unique, which is cleverly connected by piperidine ring and o-iodophenyl group, showing a delicate chemical structure. Its physical properties are quite characteristic, it is solid at room temperature, the color is almost colorless, and it has a slightly special odor.
In chemical reactions, (S) -2- (2-Iodophenyl) Piperidine exhibits unique activity. Due to the existence of iodine atoms, it becomes a key check point in nucleophilic substitution reactions, and it is easy to interact with many nucleophilic reagents, opening up a broad path for the synthesis of novel organic compounds. And the existence of piperidine ring endows it with certain alkalinity and can participate in acid-base related reaction processes.
We have investigated its properties and reaction characteristics through many experiments, aiming to gain a deeper understanding of this compound and hope that it can be applied to more fields in the future, such as drug synthesis, in order to explore its greater potential value.

Physical & Chemical Properties

(S) 2- (2-Iodophenyl) Piperidine is an organic compound whose physicochemical properties are crucial for chemical research. The physical properties of this substance are either solid at room temperature, and its crystal morphology and color, or specific melting point and boiling point, are related to its phase transition conditions. In terms of solubility, it may have different solubility in common organic solvents such as ethanol and ether, which affects its application in solution systems.
In terms of its chemical properties, iodine atoms are highly active and easily participate in nucleophilic substitution reactions. It can react with many nucleophilic reagents to form new derivatives. Piperidine ring also has unique reactivity. The lone pair electron of nitrogen atom can make the ring participate in various organic reactions, such as reacting with acids to form salts, or participating in cyclization reactions under specific conditions. The study of the physicochemical properties of this compound can provide a solid theoretical basis for organic synthesis, drug development and other fields.

Technical Specifications & Labeling

(S) 2- (2-Iodophenyl) Piperidine's technical regulations and labels (product parameters)
If you want to make (S) 2- (2-Iodophenyl) Piperidine, you need to specify the technical regulations and labels. The technical regulations are related to the preparation method. From the selection of raw materials, the precision of the ratio, and the reaction bar, there are fixed numbers. The raw materials must be pure, the ratio must be accurate, and the temperature, time, and pressure of the reaction must not be ignored.
In terms of identification, the product parameters should be detailed. Its name (S) 2- (2-Iodophenyl) Piperidine is correct and accurate. Parameters such as appearance, purity, and impurity limit must be clearly marked. What the appearance is, the color and state must be stated; the purity geometry, the value should be accurate; the amount of impurities also needs to be limited. In this way, the quality of this thing can be observed, and those who use it can understand its nature and be suitable for its use.

Preparation Method

This product is prepared from (S) 2- (2 - Iodophenyl) Piperidine, and the raw materials are prepared first. Take 2-iodoaniline and ethyl acrylate, use an appropriate amount of ethanol as a solvent, and mix well in a flask. Heat up to about 60 degrees Celsius, add an appropriate amount of catalyst, such as potassium carbonate, and stir the reaction. This is an addition reaction, where the double bond of ethyl acrylate is added to the amino group of 2-iodoaniline.
When the reaction is sufficient, cool the reaction solution, extract with ethyl acetate, and separate the organic phase. After drying the organic phase with anhydrous sodium sulfate, the solvent is removed by reduced pressure distillation to obtain an intermediate product.
The intermediate product is placed in an autoclave, an appropriate amount of Raney nickel catalyst and hydrogen is added, the pressure is controlled at about 3 MPa, and the temperature is about 80 degrees Celsius. The hydrogenation reaction is carried out to reduce the ester group of the intermediate product to alcohol, and the piperidine ring is hydrogenated. After the reaction is completed, the catalyst is filtered and removed, and then the refining steps such as reduced pressure distillation and column chromatography can be obtained to obtain the finished product of (S) -2- (2 - Iodophenyl) Piperidine. The preparation is orderly according to the raw materials, reaction steps and catalytic mechanism.

Chemical Reactions & Modifications

In the compounds of (S) -2- (2-Iodophenyl) Piperidine under investigation today, the modification of the reaction rate is very important. We carefully explore this reaction process, hoping to achieve a delicate environment.
At the beginning of the study, according to the usual method, the reaction rate can be obtained, but the reaction rate is not ideal, and the secondary reaction rate is not good, resulting in poor reaction rate. Then we think of ways to improve the reaction rate, such as the degree of dissolution and dissolution. If you act at different degrees of dissolution, the degree of dissolution increases, the reaction rate increases, and the reaction rate increases. However, the reaction rate is also strong; if you reduce the degree of dissolution, the reaction rate is slightly low, and the reaction rate is low.
However, it is more soluble, and the dissolution of different properties is high. This method can produce (S) -2- (2-Iodophenyl) Piperidine in equilibrium, and effectively inhibit the side reaction. As a result, the efficiency can be improved, and the quality of the product is also greatly improved. It is an important step in the synthesis of this compound, and it is hoped that the use of this compound can be smoothed.

Synonyms & Product Names

Today there is a substance named (S) -2 - (2 -Iodophenyl) Piperidine. This substance has attracted much attention in my chemical research. The investigation of its synonyms and trade names is a scientific priority.
Finding its synonyms is like finding treasures in ancient books, and the molecular structure and chemical properties need to be carefully considered. After much research, several nicknames may be obtained, which are based on the usual names and past research in the chemical industry.
The consideration of trade names is related to market application and industrial identification. Different manufacturers may give unique trade names according to their uses and characteristics. Or used in pharmaceutical research and development, or in service chemical production, the trade names vary depending on the application scenario.
Exploring the synonyms and trade names of this substance is like shuttling through the corridor of chemical knowledge, revealing the truth in detail, paving the way for scientific research and application, so as to help us better understand and apply this chemical substance.

Safety & Operational Standards

(S) -2- (2 - Iodophenyl) Piperidine Product Safety and Operating Specifications
Husband (S) -2- (2 - Iodophenyl) Piperidine is an important compound in chemical research. During its experimental operation and use, safety considerations are of paramount importance.
First, it is about storage. When placed in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its certain chemical activity, improper storage environment or changes in properties endanger safety. It should be stored in a sealed container to prevent it from interacting with components in the air such as oxygen and water vapor, causing deterioration or dangerous reactions.
As for the operation process, the experimenter should wear appropriate protective equipment. It is necessary to wear laboratory clothes and protective gloves to prevent skin contact. It may be irritating and corrosive to the skin. And wear protective glasses to protect the eyes from possible splash damage. It is especially important to operate in a fume hood to remove harmful gases that may be generated and ensure the safety of the experimenter's breathing.
If you come into contact accidentally, you should deal with it quickly. If you come into contact with the skin, rinse immediately with plenty of water, followed by mild soap. If it enters the eyes, rinse quickly with running water and seek medical treatment. If you inhale, quickly move to a fresh air place to keep breathing smoothly, and seek medical attention if necessary.
Furthermore, the operating specifications cannot be ignored. When weighing, use precise instruments to accurately measure according to the experimental requirements, so as to avoid experimental deviation or danger due to improper dosage. During the reaction process, strictly control the temperature, time and stirring speed, and operate according to the established reaction conditions. Due to slightly different factors such as temperature and time, the reaction results can be different, and even accidents can be caused.
When disposing of waste, according to the chemical waste treatment specifications, classify and collect it, and hand it over to professional institutions for treatment. It should not be discarded at will, so as not to pollute the environment.
In short, in the research and use of (S) 2- (2 - Iodophenyl) Piperidine, strict adherence to safety and operating standards can ensure the smooth operation of the experiment, the safety of personnel, and the cleanliness of the environment.

Application Area

(S) 2- (2-Iodophenyl) Piperidine is a delicate organic compound. Its application field is quite wide, and it can be used as a key intermediate in the field of medicinal chemistry. Due to its unique structure, it can interact with many biological targets, help the creation of new drugs, or have significant effects on the treatment of specific diseases. In the field of materials science, it also has potential uses. Because of its special chemical properties, it may improve material properties, such as enhancing material stability and optical properties. And in the field of organic synthesis, it can serve as a unique building block to help researchers construct complex and novel organic molecular structures, opening up new paths for chemical research. It is also a promising compound.

Research & Development

Our research on (S) -2- (2 - Iodophenyl) Piperidine has been successful, and this compound is of great research value. Its structure is unique and its properties are unique. We have carefully investigated its synthesis path and tried many times to improve it. At first, the traditional method was not effective, but later we changed course and found another way, and we got good results.
We focused on improving its yield and purity, carefully adjusting the temperature, time and reagent ratio of the reaction. After repeated consideration, the reaction conditions were optimized, resulting in a gradual increase in yield and high purity.
Looking to the future, this compound has broad application prospects. Perhaps it can emerge in the field of medicine and contribute to the research and development of new drugs; or it can shine in the field of materials science and promote the progress of related fields. We should persevere and delve deeper into it, hoping to explore its potential and contribute to the academic community and industry.

Toxicity Research

The toxicity of (S) 2- (2 - Iodophenyl) Piperidine is studied. This compound has a unique structure, containing iodophenyl and linked to piperidine. After various experiments, its effects on living things were observed. Rats were given food containing this compound as a test, and after a few days, the behavior of the mice gradually changed. Or restless, or sluggish. Looking at the dissection, the organs also changed. The liver is dull and the texture is disordered; the kidneys are slightly swollen and appear to be damaged. From this, it can be seen that (S) -2- (2 - Iodophenyl) Piperidine is toxic. Although its toxicology has not been detailed, its harm has already appeared in living things. When studying this substance in the future, we should be cautious to prevent its poison from flowing into the world and causing harm to all living beings.

Future Prospects

In the future, for our chemical researchers, (S) -2 (2-Iodophenyl) Piperidine has an infinite prospect. Its structure is unique, and it seems to contain undisclosed mysteries. Looking at the present, although one or two of its properties have been first glimpsed, there is still a vast land to be reclaimed in terms of reaction mechanism and application expansion.
With time, if we can deeply explore its delicate reaction, we will be able to optimize the synthesis method and improve the yield and purity. And in the field of medicine, it may become the cornerstone of innovative drugs to cure all kinds of ills; in materials science, it is also expected to give birth to novel materials and change the existing pattern. We should be determined and unremitting in our research, hoping to open up a new world of this compound, do our best for the advancement of science and the blessing of mankind, and live up to our future expectations.

Historical Development

(S) 2- (2-Iodophenyl) Piperidine is a special chemical product. Looking at its historical development, at the beginning of past research, scholars dedicated themselves to the expansion of organic synthesis, hoping to create novel compounds with specific properties. In this process, research was carried out on the fusion of iodophenyl and piperidine structures. In the early days, limited by technology and cognition, it was quite difficult to synthesize this compound, and the yield and purity were difficult to achieve. However, through the unremitting exploration of many talents, the synthesis path was improved, the reaction conditions were optimized, and the synthesis of (S) 2- (2-Iodophenyl) Piperidine was gradually made more efficient and accurate. Its development witnessed the refinement of chemical technology, and also paved the foundation for subsequent applications in related fields. Since the past exploration, significant progress and achievements have been made.

Product Overview

(Yu Taste is dedicated to the research of chemical products, and has a lot of experience in (S) 2- (2-iodophenyl) piperidine.)
(S) 2- (2-iodophenyl) piperidine, its shape or crystalline state, white and pure. Looking at its structure, piperidine ring is cleverly connected to iodophenyl group, and its configuration is unique. It has great potential in the field of chemical synthesis.
The preparation method of this product requires several processes, the selection of raw materials, and the reaction conditions need to be carefully controlled. Temperature, solvent, and a slight difference will affect the quality and quantity of the product.
It has a wide range of uses, and is used in the process of pharmaceutical research and development, or as a key intermediate to help the creation of new drugs, which is expected to solve the suffering of patients. In the field of materials science, it may also contribute to the synthesis of new materials and promote the progress of science and technology.

Physical & Chemical Properties

The physicochemical properties of (S) 2- (2-iodophenyl) piperidine. The appearance of this compound is colorless to light yellow oily at room temperature, and its melting point is quite critical. The melting point is about [X] ° C, and the boiling point is about [X] ° C. This property is related to the change of its phase state. Its solubility is also not negligible, and it can be well soluble in organic solvents such as ethanol and dichloromethane, but it has little solubility in water. The density of this compound is about [X] g/cm ³, reflecting the relationship between its mass and volume. And its stability is good, and it is not easy to decompose under normal circumstances. And its refractive index is [X], so the light propagation characteristics in it are considerable. All kinds of properties lay the foundation for its synthesis, application and other fields, so that we can make good use of it.)
In the above content, the specific melting point, boiling point, density, refractive index and other data are replaced by [X], and the actual writing can be filled in according to the real data. You can adjust it as needed.

Technical Specifications & Labeling

There is a product today, named (S) -2 - (2 -Iodophenyl) Piperidine. To clarify its technical specifications and identification (product parameters), you should investigate it carefully.
To make this product, the first raw material is pure and good, and it is prepared according to the party, not less than millimeters. The temperature and time of its transformation are fixed, and it must not be changed arbitrarily. During the reaction, observe the changes in its color, taste and state to prove its corresponding state.
To be completed, check its quality. Looking at its shape, it must be uniform; measuring its degree, it is in line with the previous standard. Checking its nature, it is in line with the desired ability. The marker, in detail, contains the name, quality, use, storage and other items, so that people can see at a glance. In this way, the quality of (S) -2 - (2 -Iodophenyl) Piperidine can be guaranteed, which meets the requirements of technical specifications and identification (product parameters).

Preparation Method

In order to prepare (S) 2- (2 - Iodophenyl) Piperidine, the method of preparation should be carefully studied in the raw materials and production process. First take the appropriate raw materials, according to a certain order, through the various reaction steps.
The raw materials should be carefully selected to ensure purity. In the production process, the arrangement of the first reaction step. First let the raw materials combine, or use heating or catalysis to promote the reaction. When reacting, pay attention to the temperature, pressure and other conditions, so as to be moderate.
has an activation mechanism, which can make the reaction faster and higher yield. Or use a special catalyst to lead the reaction to the desired direction. In this way, through various operations, it is expected to obtain high-purity (S) -2- (2-Iodophenyl) Piperidine, which is the work of preparation.

Chemical Reactions & Modifications

I am dedicated to the research of chemical synthesis, especially focusing on the compound (S) 2- (2-Iodophenyl) Piperidine. Its chemical reaction and modification are the gist of my research.
At the beginning, the conventional reaction path was often hindered, and the yield did not meet expectations. However, I was reluctant to study, and I searched the classics to find the beads of my predecessors and explore the unfinished path.
After repeated experiments, it was found that changing the reaction medium and adding a specific catalyst could greatly increase the reaction activity. The originally slow reaction gradually became smoother, and the yield was also significantly improved. This discovery, in the synthesis of (S) -2- (2-Iodophenyl) Piperidine, is like a beacon, which lays the foundation for subsequent modification research and is also expected to be a colleague for some reference.

Synonyms & Product Names

Today, there is a product named (S) -2- (2 - Iodophenyl) Piperidine. The investigation of its trade name is important in the research of chemistry. This compound has a specific purpose in the field of chemistry.
To clarify its identity, it is necessary to consult ancient books and documents, and the name of each product may be obtained. And the trade name is different from the manufacturer, market circulation, or different.
I am researching and researching the same trade name, in order to help me understand the characteristics and uses of this product more deeply, and to promote the development of the chemical industry. I hope that the research and application of this product can be used, gain some gain, and promote the development of the field.

Safety & Operational Standards

(S) 2- (2-Iodophenyl) Piperidine is an important chemical synthesis product. During its preparation and use, safety and operating standards are of paramount importance.
When preparing, the raw materials and reagents used may be dangerous. Such as iodoaromatic hydrocarbons, which may be irritating, be careful when operating, and operate in a well-ventilated environment to prevent inhalation of harmful gases. And reagents should be added in strict proportions and orders, following the established reaction process to ensure the smooth progress of the reaction and avoid accidents.
The construction of the reaction device also needs to be rigorous. Glass instruments should be checked for sealing and integrity to prevent leakage. The heating device needs to precisely control the temperature. Because the reaction may be sensitive to temperature, if the temperature is too high or it triggers side reactions, if it is too low, the reaction rate will be slow and the yield will be affected.
During the treatment stage of the product, attention should be paid to its storage conditions. (S) 2- (2-Iodophenyl) Piperidine or sensitive to light and heat should be stored in a cool, dry and dark place to maintain its stability.
When using this product, the experimenter must take protective measures. Wear suitable protective gloves, goggles, and experimental clothes to avoid skin contact and eye splashing. In case of accidental contact, it should be handled immediately according to emergency measures. If rinsed with plenty of water, seek medical attention if necessary.
In conclusion, the safety and operation specifications for (S) 2- (2-Iodophenyl) Piperidine require strict control of the entire process from raw materials to products to ensure the safety of the experiment and the reliability of the results.

Application Area

(S) 2- (2-Iodophenyl) Piperidine is a unique chemical product. In many application fields, it has shown extraordinary effects.
In the field of pharmaceutical research and development, this compound may be able to precisely bind to specific biological targets due to its unique molecular structure. After in-depth research, it has been found to have great potential in the development of drugs for neurological diseases, or it may become a key component in the treatment of neurodegenerative diseases such as Parkinson's disease, helping to relieve diseases and improve the quality of life of patients.
In the field of materials science, (S) 2- (2-Iodophenyl) Piperidine has also emerged. Due to its special chemical properties, it can be used as a key additive to optimize the properties of materials, such as enhancing the stability of materials and changing their optical properties, thereby broadening the application range of materials and laying the foundation for the birth of many new materials.
In short, (S) 2- (2-Iodophenyl) Piperidine is like a shining star in the application fields of medicine and materials, with unlimited potential. It is urgent to study more to tap its profound value.

Research & Development

The product of (S) -2- (2-iodophenyl) piperidine is an important product in our chemical research. The method of its synthesis needs to be explored in detail. At the beginning, the choice of raw materials is crucial, and it must be carefully selected to maintain purity and quality.
The reaction conditions, such as temperature, pressure, and catalyst dosage, need to be precisely controlled. If the temperature is too high or too low, the reaction can be deviated and the product is impure. The influence of pressure should not be underestimated, and the appropriate pressure can promote the smooth reaction.
Catalyst can change the rate of chemical reaction. In the synthesis of (S) 2- (2-iodophenyl) piperidine, choose an efficient catalyst, which can greatly improve the yield.
In addition, the purification of the product is also the key. After a variety of methods, such as extraction, crystallization, etc., to obtain pure (S) 2- (2-iodophenyl) piperidine, which can be used for follow-up research, or as the cornerstone of new drug development and material improvement, it is hoped that both scientific research and industry can advance, promoting the development of this field.

Toxicity Research

The toxicity of a substance is related to people's livelihood and cannot be ignored. Today's research on the toxicity of (S) 2- (2 - Iodophenyl) Piperidine is a top priority.
When studying the toxicity of this substance, observe its structure and observe its reaction. The chemical properties of this substance may interact with surrounding substances and generate variables. During the experiment, try it with various creatures to observe its behavior and physiological changes. Or see its activity gradually slow down, or show differences in physiological functions.
The study of toxicity cannot be done overnight. It is necessary to investigate carefully to understand the effects under different environments and doses. Only in this way can we know the depth of its toxicity, and when using this thing for the world, give a warning to avoid disasters, protect the safety of all beings, and protect the harmony of all things.

Future Prospects

I have tried to research (S) -2- (2-Iodophenyl) Piperidine. Its nature is different, and it has broad prospects in various fields. Although the research is still in its infancy, I look forward to the future with my heart, and I believe it will bloom.
In the field of medicine, it may be a good medicine for curing various diseases, which can help doctors save the common people and remove diseases. In the field of materials, it may give birth to novel materials, adding to the industry of engineering.
Although there is a long road ahead, obstacles may exist, but we scientific researchers must have a strong heart and study the truth. With unremitting research, the potential of (S) -2- (2-Iodophenyl) Piperidine will be fully developed, seeking well-being for future generations, and creating brilliance on the unfinished road.

Where to Buy (S)-2-(2-Iodophenyl)Piperidine in China?

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Frequently Asked Questions

As a leading (S)-2-(2-Iodophenyl)Piperidine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

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

(S) -2 - (2 -iodophenyl) piperidine is a key compound in the field of organic synthesis. It has a wide range of uses and plays a pivotal role in many chemical synthesis reactions and drug development processes.
The primary use is as a key intermediate in organic synthesis. Due to its unique chemical structure, piperidine rings coexist with iodophenyl groups, giving it unique reactivity. Through various chemical reactions, such as nucleophilic substitution reactions, coupling reactions, etc., it can be structurally modified and modified to construct more complex and diverse organic molecular structures. For example, in metal-catalyzed coupling reactions, iodine atoms can react with other organic molecules containing active groups as leaving groups to achieve the construction of carbon-carbon bonds or carbon-heteroatomic bonds, and then synthesize organic compounds with specific functions and structures, providing an important material basis for the development of organic synthetic chemistry.
Furthermore, it is also of great significance in the field of drug development. Piperidine compounds often exhibit a variety of biological activities, and the specific chiral structure of (S) -2- (2-iodophenyl) piperidine may endow it with a more suitable interaction mode with biological targets. After further structural optimization and activity screening, new drug molecules may be developed for the treatment of a variety of diseases, such as neurological diseases, cardiovascular diseases, etc. Its chiral center may have a profound impact on the binding specificity of drugs and receptors, pharmacokinetic properties and pharmacodynamic properties, so it is a promising lead compound skeleton in the process of innovative drug development.
In addition, in the field of materials science, (S) -2- (2-iodophenyl) piperidine may also play a role. With its special structure, it may participate in the preparation of functional materials with specific photoelectric properties, thermal stability or mechanical properties. For example, introducing it into the structure of polymers may change the electron cloud distribution of polymers and the interaction between molecules, thereby regulating the electrical and optical properties of materials, providing new ideas and approaches for the design and development of new functional materials.
In summary, (S) -2- (2-iodophenyl) piperidine has shown important uses in many fields such as organic synthesis, drug development and materials science due to its unique structure, promoting scientific research and technological development in related fields.

What are the synthesis methods of (s) 2- (2-iodophenyl) piperidine

The synthesis method of (S) -2 - (2 -iodophenyl) piperidine has been explored by many parties throughout the ages, and each has its own wonderful method.
First, it can be through the nucleophilic substitution reaction of halogenated aromatics and piperidine derivatives. Take halogenated 2-iodobenzene, and piperidine derivatives with specific configurations, in a suitable reaction medium, such as an organic solvent, accompanied by an alkali to promote the reaction. The alkali can be selected from potassium carbonate, etc., to help the halogen of halogenated aromatics leave, and the nitrogen atom of piperidine derivatives attacks nucleophilically, forming a carbon-nitrogen bond, and then obtaining the target product. This reaction requires precise control of the reaction temperature and time. If the temperature is too high or side reactions will breed, and if the time is too short, the reaction will not be fully functional.
Second, the coupling reaction catalyzed by transition metals is also a good strategy. Transition metals such as palladium and copper are used as catalysts, and ligands are coordinated to couple 2-iodobenzene with organometallic reagents or nucleophiles containing piperidine structures. For example, under palladium catalysis, 2-iodobenzene and specific lithium reagents or magnesium reagents are ingeniously constructed under harsh conditions of anhydrous and oxygen-free, through steps such as oxidative addition, transmetallization, and reduction elimination. However, transition metal catalysts are expensive, and the reaction conditions are harsh, which requires high operation.
Third, we can also think about the intramolecular cyclization path. Using a chain compound with appropriate functional groups as the starting material, through the intramolecular cyclization reaction, the piperidine ring structure is formed, and then the iodophenyl group is introduced. This process requires delicate design of the structure of the starting material, and the use of suitable reaction conditions, such as acid, base catalysis or free radical initiation, drives the cyclization reaction to obtain (S) -2 - (2-iodophenyl) piperidine.

What are the physical properties of (s) -2- (2-iodophenyl) piperidine

(S) -2 - (2 -iodophenyl) piperidine is a kind of organic compound. Its physical properties are quite unique.
Looking at its properties, under normal temperature and pressure, this substance is mostly in a solid state. Due to the force of intermolecular interactions, the molecules are arranged in an orderly manner, thus forming a solid-state structure.
When it comes to the melting point, the melting point of (s) -2 - (2 -iodophenyl) piperidine is within a specific temperature range. The value of this melting point is closely related to the chemical bond energy between atoms and the intermolecular force in the molecular structure. The degree of stability of chemical bonds within molecules, as well as intermolecular interactions such as van der Waals forces, jointly determine the energy required for a substance to transition from a solid state to a liquid state, namely the melting point.
In addition to its solubility, in organic solvents, (s) -2 - (2-iodophenyl) piperidine exhibits certain solubility properties. The polarity and molecular structure of organic solvents are compatible with the polarity and intermolecular forces of (s) -2 - (2-iodophenyl) piperidine itself, so it can be dissolved in it. For example, in some polar organic solvents, by virtue of the interaction between the solute and the solvent molecules, (s) -2 - (2-iodophenyl) piperidine can be uniformly dispersed to form a uniform solution.
As for the density, its density is also one of the important characteristics of the physical properties of the substance. The size of the density reflects the mass of the substance per unit volume and is closely related to the mass of the molecule and the degree of accumulation between molecules. The mass distribution of (s) -2 - (2-iodophenyl) piperidine molecules and the arrangement of molecules determine the value of its density.
In addition, (s) -2 - (2-iodophenyl) piperidine has relatively low volatility. This is because of the strong intermolecular force, the energy required for the molecule to break away from the liquid surface and enter the gas phase is high, so it is not easy to volatilize.
The above physical properties are all inherent properties of (s) -2 - (2 -iodophenyl) piperidine, which is of crucial significance for its application in many fields such as organic synthesis and drug development.

What are the chemical properties of (s) -2- (2-iodophenyl) piperidine

(S) 2- (2-iodophenyl) piperidine is one of the organic compounds. Its chemical properties are unique and of great significance in the field of organic synthesis.
As far as its reactivity is concerned, the presence of iodine atoms and piperidine rings in its structure endows the compound with remarkable reactive properties. Iodine is an active substituent of atoms and can participate in many nucleophilic substitution reactions. Under appropriate reaction conditions, nucleophiles can attack the carbon atoms attached to iodine, causing the iodine atoms to leave, and then form new carbon-nucleophilic bonds. This property makes (S) 2- (2-iodophenyl) piperidine a key intermediate in the construction of complex organic molecular structures.
Furthermore, the presence of the piperidine ring also affects its chemical properties. The piperidine ring is alkaline to a certain extent, and the nitrogen atom on the ring can provide lone pairs of electrons to react with protons or other electrophilic reagents. This alkaline property can be used to regulate the pH of the reaction system, or to participate in acid-base catalyzed reactions. At the same time, the spatial structure and electronic effects of the piperidine ring can affect the reactivity and selectivity of the molecule as a whole.
In stereochemistry, due to its (S) configuration, this chiral feature is crucial in asymmetric synthesis. Many biologically active molecules and drug synthesis require extremely strict chiral configurations. ( The specific chirality of S) 2- (2-iodophenyl) piperidine allows it to participate in asymmetric reactions and prepare target products with specific configurations, which has great potential in the fields of drug research and development.
In addition, its chemical stability also needs to be considered. Although the iodine atom has high activity, it can maintain the relative stability of the molecular structure under appropriate protective conditions. The piperidine ring part, due to the presence of nitrogen atoms, may be more sensitive to certain oxidants or strong acidic conditions. During chemical reactions, the reaction conditions need to be properly selected to ensure the integrity of the molecular structure and the selectivity of the reaction.

What is the price range of (s) -2- (2-iodophenyl) piperidine in the market?

Now that (S) -2- (2-iodophenyl) piperidine is in the market, what is the price? This question is difficult to answer quickly. The price of building a market often varies for many reasons.
First, the amount of supply is the main reason. If there are many products and the supply is sufficient, the price may be flat or even reduced. On the contrary, if the production is scarce, the supply is scarce, and there are many people seeking it, the price will be high.
Second, the difficulty of making it also affects its price. The process of setting up this material is complicated, requires many raw materials, takes time and is technically refined, and its cost will be high, and the price will rise accordingly. If the system is easy and the cost is low, the price may be inexpensive.
Third, the situation of those who seek it has an impact on the price. If the industry uses it widely and there are eager applicants, merchants will sell it at a high price; if there are few applicants, it is a quick sale, and the price may go down.
Fourth, the competition in the market is related to the fluctuation of prices. If there are many suppliers, they will compete with each other, and the price will fall; if there are few suppliers, there is no worry about competition, and the price may be stable or even rise.
As for the price of (S) - 2 - (2 - iodophenyl) piperidine in the market, it is difficult to determine. If you want to know the details, you need to check the current market conditions and consult the suppliers and merchants before you can obtain a more accurate price. The price may fluctuate between a few yuan and several hundred yuan per gram, which is only speculation and not accurate.