3 Bromo 1h Pyrrolo 2 3 C Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3-bromo-1H-pyrrolo[2,3-c]pyridine

    Specifications

    HS Code

    635446

    Chemical Formula C7H5BrN2
    Molar Mass 197.03 g/mol
    Appearance Solid (predicted)
    Melting Point N/A (no common data found)
    Boiling Point N/A (no common data found)
    Solubility In Water Low (due to non - polar nature of aromatic rings)
    Density N/A (no common data found)
    Pka N/A (no common data found)
    Logp Predicted to be relatively high due to hydrophobic rings
    Stability Stable under normal conditions, but can react with strong oxidizing and reducing agents

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    General Information
    Where to Buy 3-bromo-1H-pyrrolo[2,3-c]pyridine in China?
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    Frequently Asked Questions

    As a leading 3-bromo-1H-pyrrolo[2,3-c]pyridine 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 3-bromo-1H-pyrrolo [2,3-c] pyridine
    3-Bromo-1H-pyrrolo [2,3-c] pyridine is an organic compound with unique chemical properties. Its appearance is usually solid, and the exact color varies depending on the purity and preparation method. It is usually a white to pale yellow solid.
    When it comes to physical properties, the melting point, boiling point and solubility are quite important. The melting point determines the temperature at which the compound changes from solid to liquid state, but the specific value is determined by precise experiments. The boiling point is related to the temperature conditions for changing from liquid to gas state. In terms of solubility, in common organic solvents such as dichloromethane, chloroform, N, N-dimethylformamide (DMF), it may exhibit good solubility and low solubility in water due to the lack of groups that can effectively form hydrogen bonds with water in its molecular structure.
    Chemically, the reactivity of 3-bromo-1H-pyrrolo [2,3-c] pyridine attracts attention. As an active functional group, bromine atoms can participate in many chemical reactions. First, in nucleophilic substitution reactions, bromine atoms can be replaced by other nucleophiles, such as alkoxy, amino, etc., to form new carbon-heteroatom bonds, laying the foundation for the synthesis of complex organic molecules. Second, in the metal-catalyzed coupling reaction, under the action of metal catalysts such as palladium and nickel, it can be coupled with substrates containing alkenyl groups and aryl halides to form carbon-carbon bonds, which is widely used in the fields of medicinal chemistry and materials science. Third, the intramolecular pyridine and pyrrole parts endow it with alkalinity and can react with acids to form salts, which affects its stability and reactivity in different acid-base environments.
    In the field of organic synthesis, 3-bromo-1H-pyrrolo [2,3-c] pyridine is often used as a key intermediate. In drug development, or participate in the construction of biologically active molecular structures, because pyridine and pyrrole structural units are commonly found in many drug molecules, they are of great significance for regulating the interaction between drugs and biological targets.
    In conclusion, the chemical properties of 3-bromo-1H-pyrrolo [2,3-c] pyridine make it important in organic synthesis, pharmaceutical chemistry and other fields, providing an effective tool for chemists to explore new compounds and develop innovative drugs.
    What are the common synthesis methods of 3-bromo-1H-pyrrolo [2,3-c] pyridine
    3-Bromo-1H-pyrrolo [2,3-c] pyridine is an important organic compound, and its common synthesis methods include the following:
    First, it is prepared by nucleophilic substitution reaction using nitrogen-containing heterocycles as the starting material. First, take a suitable pyridine derivative and make it meet the brominating agent under specific reaction conditions. If pyridine is used as the substrate, in the presence of a suitable solvent and base, it undergoes nucleophilic substitution with bromine, and bromine atoms can be introduced at specific positions in the pyridine ring. This step requires strict control of the reaction temperature, time and proportion of reactants to prevent side reactions. After that, the pyrrolido-pyridine structure is constructed by ring-off reaction. This process often requires the help of suitable catalysts, such as metal catalysts or organic small molecule catalysts, to promote the formation of intra-molecular rings, so as to obtain the target product 3-bromo-1H-pyrrolo [2,3-c] pyridine.
    Second, synthesize by cyclization reaction. Select a chain compound with a suitable functional group, first make the chain molecule through a specific reaction, and build a cyclic activity check point in the molecule. For example, through the reaction of halogenated hydrocarbons and nitrogen-containing compounds, an intermediate with a suitable connecting arm is formed. Then, under suitable reaction conditions, through molecular cyclization, the pyrrolidine structure is constructed in one step, and bromine atoms are introduced at the same time. This method requires careful design of the structure of the starting material to ensure that the cyclization reaction can proceed smoothly, and the bromine atoms can be precisely introduced into the target position.
    Third, a coupling reaction catalyzed by transition metals is used. Halogenated pyridine and a halogen containing pyrrole structure are used as raw materials, and a coupling reaction occurs under the action of a transition metal catalyst such as a palladium catalyst. This reaction requires the selection of suitable ligands to enhance the activity and selectivity of the catalyst. At the same time, the reaction solvent, base and reaction temperature conditions also need to be carefully regulated. Through the coupling reaction, pyridine can be connected to the pyrrole structure to obtain 3-bromo-1H-pyrrolo [2,3-c] pyridine. And this method can better control the position and selectivity of the substituents, which is conducive to the synthesis of the target product.
    In which fields is 3-bromo-1H-pyrrolo [2,3-c] pyridine used?
    3-Bromo-1H-pyrrolo [2,3-c] pyridine is an important organic compound with outstanding applications in many fields.
    In the field of medicinal chemistry, this compound has shown unique value. Due to its structural properties, it can be used as a key intermediate for the synthesis of a variety of biologically active drug molecules. Many studies have focused on using it as a starting material and chemically modifying it to construct structures with specific pharmacological activities, such as the development of anti-tumor drugs. Through in-depth analysis and modification of its structure, scientists hope to obtain new drugs with high selective inhibitory effect on tumor cells, and find a new way to solve the cancer problem.
    In the field of materials science, 3-bromo-1H-pyrrolo [2,3-c] pyridine also has important applications. It can participate in the preparation of organic materials with special properties, such as photovoltaic materials. Its structure gives the material unique photoelectric properties, and can be used to fabricate devices such as Light Emitting Diodes (LEDs) and organic solar cells. In these applications, the compound helps to improve the performance of devices, such as improving the photoelectric conversion efficiency, enabling solar cells to convert light energy into electricity more efficiently, and promoting the development of renewable energy technologies.
    Furthermore, in the field of organic synthetic chemistry, this compound serves as a unique structural unit and provides an effective strategy for synthesizing complex organic molecules. Chemists use their active reaction check points to construct organic compounds with diverse structures through various organic reactions, such as nucleophilic substitution reactions and metal catalytic coupling reactions, to expand the boundaries of organic synthesis and lay the foundation for the creation of new functional materials and bioactive molecules.
    What are the physical properties of 3-bromo-1H-pyrrolo [2,3-c] pyridine
    3-Bromo-1H-pyrrolo [2,3-c] pyridine is an organic compound. Looking at its physical properties, under normal temperature and pressure, this substance is usually in a solid state. Due to the relatively strong intermolecular forces, the molecules are closely arranged and maintain the solid state structure. The value of its melting point is related to the lattice stability and lattice energy of the molecule. The specific melting point data can be obtained by experimental measurement. In the process of chemical synthesis and purification, the knowledge of the melting point is extremely critical, and the purity of the substance can be determined based on it.
    Regarding solubility, this compound exhibits certain solubility in common organic solvents such as dichloromethane, chloroform, N, N-dimethylformamide, etc. In dichloromethane, the polarity of dichloromethane interacts with some groups of the compound, so that the molecule can be dispersed in the solvent. However, in water, its solubility is not good, because the polarity of water is quite different from the overall polarity of the compound, and the compound lacks groups that strongly interact with water molecules, such as a large number of hydroxyl groups, carboxyl groups, etc.
    The color state of the compound is often white to light yellow solid. The appearance of this color is due to the characteristics of electron transition in the molecular structure. The conjugated system contained in its molecular structure makes electrons transition after absorbing light of a specific wavelength, thereby reflecting light of a specific color, which is perceived by the human eye.
    Its density is also one of the important physical properties. The density reflects the mass of the substance per unit volume, which is of great significance for the calculation of its dosage in a specific reaction system and the analysis of stratification in the mixed system. It can be accurately measured by experimental means using density measuring instruments.
    In addition, its volatility is relatively low. Due to the interaction between molecules such as van der Waals force, molecules need to overcome large energy to break away from the condensed phase and enter the gas phase, so the volatility is limited. This characteristic has a significant impact during storage and use, which can reduce the loss caused by volatilization and the impact on the environment.
    What is the market outlook for 3-bromo-1H-pyrrolo [2,3-c] pyridine?
    3-Bromo-1H-pyrrolo [2,3-c] pyridine is one of the organic compounds. Looking at its market prospects, various factors are intertwined, resulting in complex and changeable prospects.
    From the perspective of pharmaceutical research and development, such compounds have potential medicinal value. Due to their unique chemical structure, they may be able to emerge in the creation of new drugs, such as participating in the synthesis of specific target drugs. However, the road to new drug development is long and requires many rigorous tests, from laboratory research to pre-clinical evaluation to human clinical trials, each step is thorny, time-consuming and expensive. Only a few with outstanding characteristics have the opportunity to be recognized by the pharmaceutical market. Therefore, although there are opportunities in the development of pharmaceutical applications, there are also huge challenges.
    In the field of materials science, 3-bromo-1H-pyrrolo [2,3-c] pyridine may be used as a synthetic raw material for special functional materials. With the advance of science and technology, the demand for special performance materials is increasing, such as optoelectronic materials, semiconductor materials, etc. If this compound can be chemically modified to exhibit unique electrical and optical properties, it will be able to gain a place in the materials market. However, the research and development of materials needs to take into account the performance, cost and feasibility of production processes. Whether this compound can meet the requirements of large-scale production and application remains to be further explored.
    Furthermore, the market competition situation is also a key factor. The field of organic synthetic chemistry is active, and many scientific research institutions and enterprises are committed to the research and development and application of new compounds. If other similar structural or functional compounds take the lead and occupy the market share, it will be difficult for 3-bromo-1H-pyrrolo [2,3-c] pyridine to stand out. And fluctuations in raw material supply and prices will also affect its marketing activities. If raw materials are scarce or prices are unstable, production costs will be difficult to control and market competitiveness will be weakened.
    In general, although 3-bromo-1H-pyrrolo [2,3-c] pyridine has potential applications in fields such as medicine and materials, it faces many problems such as R & D challenges, market competition and raw material supply. Only by overcoming many difficulties can it bloom in the market. Its future road, opportunities and challenges coexist.