1h Pyrrolo 2 3 B Pyridine 4 Chloro 2 Iodo
pyridine pyrrole pyrazine piperidine piperazine

1H-pyrrolo[2,3-b]pyridine, 4-chloro-2-iodo-

    Specifications

    HS Code

    767703

    Chemical Formula C7H4ClIN2
    Molecular Weight 294.48
    Appearance Solid (likely, based on similar compounds)
    Physical State At Room Temp Solid
    Boiling Point Estimated to be relatively high due to its aromatic nature
    Solubility In Water Low solubility in water as it is a non - polar aromatic compound
    Solubility In Organic Solvents Good solubility in common organic solvents like dichloromethane, chloroform
    Odor No specific odor data available, but likely odorless or with a faint, organic smell
    Density No specific density data available, but expected to be in the range of typical organic solids

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    General Information
    Where to Buy 1H-pyrrolo[2,3-b]pyridine, 4-chloro-2-iodo- in China?
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    Frequently Asked Questions

    As a leading 1H-pyrrolo[2,3-b]pyridine, 4-chloro-2-iodo- 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 chemical properties of 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-iodine-
    1H-pyrrolido [2,3-b] pyridine, 4-fluoro-2-methyl, is one of the organic compounds. Its chemical properties are unique, let me tell you in detail.
    In this compound, the structure of pyrrolido [2,3-b] pyridine endows it with a specific electron cloud distribution and spatial configuration. The fused pyrrole ring and the pyridine ring expand the conjugation system of the molecule, affecting its electron transfer and reactivity.
    In terms of its physical properties, due to the high electronegativity of fluorine atoms and methyl groups, fluorine atoms can change the polarity of the molecule, which affects its solubility and melting boiling point. Generally speaking, the solubility of fluorine-containing compounds in organic solvents may have special features.
    In terms of chemical activity, the presence of 4-fluorine atoms decreases the electron cloud density on the pyridine ring due to its electron-absorbing effect. The electron cloud density of ortho and para-sites is particularly reduced, resulting in a decrease in the activity of electrophilic substitution reaction. If there is an attack of nucleophiles, the reaction check point may tend to the relatively high electron cloud density on the pyridine ring.
    The introduction of 2-methyl increases the steric resistance of molecules. On the one hand, it affects the intermolecular force and affects the melting boiling point; on the other hand, in chemical reactions, it will interfere with the proximity of reagents to the reaction center, affecting the reaction rate and selectivity. For example, in nucleophilic substitution or electrophilic substitution reactions, the space around the methyl group is crowded, which can make it difficult for the reagents to approach, thereby changing the reaction path or reducing the reactivity.
    Furthermore, the nitrogen atom in this compound has a lone pair of electrons, which can be used as an electron donor to participate in the coordination reaction and form complexes with metal ions, etc., which may have potential applications in catalytic reactions or materials science.
    In summary, 1H-pyrrolido [2,3-b] pyridine, 4-fluoro-2-methyl compounds, whose structures interact with each other to create unique chemical properties, have research value and potential applications in organic synthesis, drug development, material preparation and other fields.
    What are the synthesis methods of 1H-pyrrolo [2,3-b] pyridine, 4-chloro-2-iodine-
    1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-amino-is an important compound in the field of organic synthesis. There are many methods for its synthesis, which are described in detail below:
    First, the method of using pyridine derivatives as starting materials. Select a specific pyridine derivative, and introduce chlorine atoms at a specific position through halogenation reaction. This requires precise control of the reaction conditions, such as temperature, solvent, catalyst, etc., according to the electron cloud distribution and reactivity of the pyridine ring, to achieve the expected halogenation check point. Then, the amination reaction is carried out with a suitable amination reagent to introduce the amino group into the designated position. In this process, the choice of amination reagents is crucial, and its nucleophilicity, reactivity and selectivity need to be considered, and the reaction conditions also need to be finely regulated to prevent side reactions.
    Second, based on the synthesis path of pyrrole derivatives. First, pyrrole derivatives containing specific substituents are prepared. Through the reactivity of pyrrole rings, they are condensed with pyridine compounds and other series of reactions to construct a pyrrolido [2,3-b] pyridine skeleton. During the condensation reaction, suitable catalysts and reaction solvents need to be selected to improve the reaction efficiency and product purity. Subsequently, according to the needs, chlorination and amination of the obtained products are carried out, and each step of the reaction needs to be strictly controlled to ensure the structure and purity of the product.
    Third, the synthesis strategy of transition metal catalysis is adopted. Transition metal catalysts play a key role in this synthesis, which can activate substrate molecules, reduce reaction activation energy, and improve reaction selectivity and efficiency. If palladium, copper and other metals are used as catalysts, with the coordination of ligands, halopyridine and aminopyrrole derivatives or vice versa can be coupled to achieve the construction of the target product. In this process, factors such as catalyst type, ligand structure, reaction temperature, and base type and dosage all have a profound impact on the reaction results, and need to be optimized through repeated experiments. When synthesizing 1H-pyrrolido [2,3-b] pyridine and 4-chloro-2-amino-, various synthesis methods have their own advantages and disadvantages. According to actual needs, such as raw material availability, cost considerations, product purity and yield requirements, etc., carefully select the appropriate synthesis path, and carefully optimize the reaction conditions of each step to achieve the ideal synthesis effect.
    What are the market application fields of 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-iodine
    The genus 1H-pyrrolido [2,3-b] pyridine, 4-fluoro-2-chlorine, is used in the market and covers many fields.
    These substances are quite useful in the field of pharmaceutical creation. Today's pharmaceutical research and development often relies on this as a basis to produce new drugs. It is particularly critical in the research and development of anti-cancer drugs. Because it can precisely act on specific targets within cancer cells, it interacts with relevant receptors or enzymes to block the proliferation, invasion and metastasis of cancer cells, and then achieves the purpose of curing cancer.
    In the agricultural and chemical industry, 1H-pyrrolido [2,3-b] pyridine and 4-fluoro-2-chlorine are also used. It can be used as a raw material for insecticides and has high-efficiency killing power against many pests. Its mechanism of action may interfere with the nervous system of pests or affect their physiological metabolism, making it difficult for pests to survive, protecting the growth of crops and reducing the infestation of diseases and pests.
    Furthermore, in the field of materials science, this compound has also emerged. Due to its unique chemical structure and physical properties, it may be used to create new types of organic materials. For example, in the preparation of optoelectronic materials, it can improve the electrical conductivity and optical properties of materials, injecting new energy into the development of electronic devices and optical instruments.
    From this point of view, 1H-pyrrolido [2,3-b] pyridine, 4-fluoro-2-chlorine have important market applications in medicine, agrochemistry, materials science and other fields, and are indeed indispensable key substances in today's chemical-related industries.
    What are the physical properties of 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-iodine-
    The physical properties of 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-methyl are as follows:
    The appearance of this compound is often in solid form, but its specific appearance may vary depending on the preparation process and purity. Under normal temperature and pressure, the stability is still good, and there is a risk of dangerous reactions when encountering hot topics, open flames or strong oxidants.
    Its melting point is of great significance for identification and purification, but the exact melting point value has not been obtained yet. The boiling point is also an important physical constant, but the exact information is also not available. < Br >
    In terms of solubility, it is generally soluble in organic solvents such as ethanol and dichloromethane. This property is crucial in the selection of reaction media and product separation and purification of organic synthesis. The solubility in water is usually poor, because its structure contains more hydrophobic hydrocarbons, and the force between water molecules is weak.
    Density is also one of the key factors to consider its physical properties. Although the exact value is unknown, it can be inferred from its structure and similar compounds that the density may be similar to that of common organic compounds.
    In addition, its physical properties such as refractive index and flash point also have a profound impact on its application in chemical production, analysis and testing, etc. However, there is a lack of clear data at present. To learn more about its exact physical properties, it is necessary to consult professional chemical literature or conduct experimental measurements.
    What are the manufacturers of 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-iodine-
    The producers of 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-methyl-this compound are quite complicated in the world. However, from the perspective of "Tiangong Kaiwu", looking at all things in the chemical industry, all those who work in this industry mostly gather in places that are good at chemical skills and have exquisite equipment.
    In the land of Huaxia and the land of the south of the Yangtze River, there are many skilled craftsmen gathered. Its water conservancy is convenient, boats and boats are connected, materials are transported conveniently, and there are many talents. Smart people are obsessed with studying the wonders of chemistry. Therefore, many workshops have arisen here, specializing in the production of this compound. They use fine methods to control the temperature and speed of reactions and seek the purity of products.
    There is also the land of Yanzhao, with a simple folk style, and craftsmen have entered this industry with determination. Although it is located in the north, with its rich minerals as a source of raw materials and unremitting practice, it can also produce high-quality 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-methyl.
    In addition, the Lingnan area has a warm climate and convenient trade. Many merchants cooperate with craftsmen to introduce advanced techniques from foreign countries and integrate with local traditional crafts, making this place an important production site for this compound. They pay attention to the needs of the market and flexibly adjust the production rules. The products they produce are sold well in China and also exported to foreign countries.
    In these places, the craftsmen are dedicated to their work, with the intention of inheritance and innovation, in the production of 1H-pyrrolido [2,3-b] pyridine, 4-chloro-2-methyl, and each can play its part to promote the output and application of this product.