4 Chloro 2 3 Dihydro 1h Pyrrolo 3 2 C Pyridine
pyridine pyrrole pyrazine piperidine piperazine

4-Chloro-2,3-dihydro-1H-pyrrolo[3,2-c]pyridine

    Specifications

    HS Code

    125841

    Chemical Formula C7H7ClN2
    Molar Mass 154.597 g/mol
    Appearance Solid (likely, based on similar compounds)
    Physical State At Room Temperature Solid
    Solubility In Water Low (expected due to non - polar nature of the pyrrole and pyridine rings)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (due to its organic nature)

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    General Information
    Where to Buy 4-Chloro-2,3-dihydro-1H-pyrrolo[3,2-c]pyridine in China?
    As a trusted 4-Chloro-2,3-dihydro-1H-pyrrolo[3,2-c]pyridine manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 4-Chloro-2,3-dihydro-1H-pyrrolo[3,2-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 4-Chloro-2,3-dihydro-1H-pyrrolo [3,2-c] pyridine
    4-Chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine is an organic compound. Its chemical properties are particularly important and it is widely used in the field of organic synthesis.
    This compound contains chlorine atoms, which have certain electronegativity and cause molecular polarity to change. The structure of the pyridine ring fused with the pyrrole ring gives the molecule a unique electron cloud distribution. The nitrogen atom of the pyridine ring has lone pairs of electrons and can participate in coordination and chemical reactions, such as nucleophilic substitution reactions. Due to the conjugation of the ring system, this compound has better stability and can participate in a variety of cyclization and addition reactions.
    In the nucleophilic substitution reaction, the chlorine atom is easily attacked by nucleophilic reagents and replaced by other groups. This property can be used to construct new carbon-carbon bonds or carbon-hetero bonds. The electron cloud distribution of its ring structure enables electrophilic substitution reactions to occur under appropriate conditions, and substituents are introduced at specific positions on the ring.
    In addition, due to its unique structure or certain biological activity, this compound can be used as a lead compound in the field of pharmaceutical chemistry. After structural modification and optimization, new drugs can be developed. And because of its active chemical properties, it can be used as a key intermediate in the synthesis of complex organic molecules. Through a series of chemical reactions, compounds with more complex structures can be constructed.
    In summary, 4-chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine is rich in chemical properties and has important application value and research potential in many fields such as organic synthesis and drug development.
    What are the synthesis methods of 4-Chloro-2,3-dihydro-1H-pyrrolo [3,2-c] pyridine
    The synthesis method of 4-chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine is ancient, and there are many kinds and ingenious.
    One method is to use a suitable pyridine derivative as the starting material and go through the halogenation step. When halogenating, it is necessary to carefully select the halogenating reagent to precisely control the reaction conditions, such as temperature, time and the proportion of the reactants. This halogenation process is related to the purity and yield of the product. It is like a craftsman carving beautiful jade, and he shows his skills in a careful manner. After halogenation, the cyclization reaction is continued to cleverly rearrange the molecular structure to build the skeleton of pyrrolido-pyridine. This cyclization reaction either requires the help of a catalyst or a specific solvent environment, which is like a pilot boat to guide the reaction in the desired direction.
    The second method is to start from the nitrogen-containing heterocyclic compound and gradually introduce chlorine atoms and construct the target structure through a multi-step reaction. The initial nitrogen-containing heterocyclic ring, or through a substitution reaction, modifies its side chain group to lay the foundation for the subsequent reaction. Then, through a series of operations such as condensation and cyclization, it is like building a delicate castle, progressing layer by layer, and finally obtaining the target product. During the reaction process, the intermediates of each step of the reaction need to be separated and identified in detail to ensure the correct reaction path.
    There are other novel strategies for synthesizing this compound. Or use the method of metal catalysis to take advantage of the unique activity and selectivity of metal catalysts to precisely achieve the formation of carbon-nitrogen bonds and carbon-chlorine bonds. This method of metal catalysis can often simplify the reaction steps and improve the reaction efficiency. However, the choice and dosage of catalysts also need to be carefully considered to prevent the growth of side reactions.
    Furthermore, or with the help of the concept of biosynthesis, simulate the chemical reaction process in the body, using enzymes as catalysts, and achieve synthesis under mild conditions. This method of biosynthesis is green and environmentally friendly, and has high selectivity. However, the acquisition of enzymes and the optimization of the reaction system are also problems that need to be overcome.
    All kinds of synthetic methods have their own advantages and disadvantages. In practical applications, careful choices should be made according to factors such as the purity, yield, and cost of the desired product.
    Where is 4-Chloro-2,3-dihydro-1H-pyrrolo [3,2-c] pyridine used?
    4-Chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine is useful in many fields such as medicine and chemical synthesis.
    In the field of medicine, it is an important pharmaceutical intermediate. It has a unique chemical structure and can participate in the construction of a variety of drug molecules. After chemical modification and reaction, compounds with specific pharmacological activities can be prepared. For example, in the development of anti-nervous system diseases drugs, derivatives constructed on this basis may play a role in the regulation of neurotransmitters, and may be potential drugs for the treatment of Parkinson's, Alzheimer's and other diseases. In the search for anti-tumor drugs, it can also play a role. It can bind to specific targets of tumor cells, or interfere with tumor cell growth signaling pathways, inhibit tumor cell proliferation, and provide new opportunities for the development of new anti-cancer drugs.
    In the field of chemical synthesis, it is a key building block of organic synthesis. Due to its structural properties, it can trigger various chemical reactions, such as nucleophilic substitution, cyclization, etc. By ingeniously designing the reaction path, complex and novel organic materials can be synthesized. In the preparation of functional polymer materials, introducing them into the polymer backbone or side chain may endow the materials with special electrical and optical properties, such as preparing polymer materials with fluorescent properties for photoelectric display, chemical sensing and other fields. And in the manufacturing of fine chemicals, it can be used to synthesize fragrances, dyes, etc., through specific reactions, to generate substances with unique flavors or colors, enhancing product quality and value.
    What is the market outlook for 4-Chloro-2,3-dihydro-1H-pyrrolo [3,2-c] pyridine
    4-Chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine, the market prospect of this product today is quite promising.
    Guanfu chemical products, emerging materials and pharmaceutical research and development are often the keys to driving the market. This pyridine derivative has extraordinary potential in the way of pharmaceutical creation. In today's world, there are frequent difficult diseases, and the demand for medicine is eager. And 4-chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine, because of its unique chemical structure, can be the cornerstone of new drug research and development, can combine with various targets in vivo, or be a sharp blade for disease resistance. Such as anti-cancer drugs, it may be able to precisely inhibit the proliferation of cancer cells and benefit patients.
    Furthermore, in the field of materials science, this compound also has potential. The search for new functional materials is a top priority at present. Its structural characteristics may endow the material with specific electrical and optical properties, which can be used to prepare high-performance electronic devices, such as organic Light Emitting Diodes, to increase its luminous efficiency and stability, in order to meet the needs of the rapid development of the electronics industry.
    However, the road to its market is not smooth. The synthesis method needs to be refined. The acquisition of high-purity products is related to cost and quality. If the cost is high, the market expansion is limited. And regulations are increasingly stringent, safety and environmental protection are all considered. Only by complying with regulations can we gain a foothold in the market.
    Although there are challenges, opportunities lie ahead. With the advance of science and technology and the increase in R & D investment, 4-chloro-2,3-dihydro-1H-pyrrole [3,2-c] pyridine will surely bloom in the market, adding to the pharmaceutical, materials and other industries, and driving the industry forward.
    What are the manufacturers of 4-Chloro-2,3-dihydro-1H-pyrrolo [3,2-c] pyridine
    4-Chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine is one of the organic compounds. In today's chemical industry, many manufacturers are involved in its production.
    One of them, such as Sigma-Aldrich, is a world-renowned chemical reagent supplier and has a good reputation in the field of fine chemicals. It produces this product and supplies it to scientific research institutions, universities and enterprises around the world to meet the needs of various experiments and production. The company's products are of high quality and diverse specifications, and can meet the requirements of different customers.
    Furthermore, TCI (Tokyo Chemical Industry Co., Ltd.) is also an important player in the production of this compound. Our company specializes in the manufacture of organic synthesis reagents, and produces 4-chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine, which is favored by the industry for its high quality and stable performance. Its products are widely used in many fields such as organic synthesis and drug research and development.
    Some domestic chemical companies are also involved in the production of this compound. They provide the market with cost-effective products by virtue of their local resource advantages and cost-effectiveness. Although the scale may not be as large as that of international manufacturers, their products can also meet the needs of some mid-to-low-end domestic markets and play an important role in promoting the development of the local chemical industry.
    In summary, the producers of 4-chloro-2,3-dihydro-1H-pyrrolido [3,2-c] pyridine include both internationally renowned giants and domestic enterprises, which together constitute the production and supply pattern of this compound to meet the diverse needs of the market.