5 Benzyl 4 5 6 7 Tetrahydro 1h Pyrrolo 3 2 C Pyridine
pyridine pyrrole pyrazine piperidine piperazine

5-benzyl-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine

    Specifications

    HS Code

    191528

    Chemical Formula C14H16N2
    Molecular Weight 212.29
    Appearance Typically a solid
    Physical State At Room Temperature Solid
    Melting Point Varies, data needed from experiment
    Boiling Point Varies, data needed from experiment
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Odor Odorless or faint odor
    Stability Stable under normal conditions
    Pka Data needed from experiment
    Logp Data needed from experiment

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    General Information
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    Frequently Asked Questions

    As a leading 5-benzyl-4,5,6,7-tetrahydro-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 is the chemical structure of 5-benzyl-4,5,6,7-tetrahydro-1H-pyrrolo [3,2-c] pyridine
    5 - benzyl - 4,5,6,7 - tetrahydro - 1H - pyrrolo [3,2 - c] pyridine is an organic compound. Looking at its naming, its chemical structure can be gradually analyzed.
    "5 - benzyl", this indicates that at the 5th position of the main structure of the compound, there is a benzyl group, and the structure of the benzyl group is -CH ² - C H, that is, a methyl group is connected to the benzene ring.
    "4,5,6,7 - tetrahydro" means that the 4,5,6,7 positions in the main structure are in a hydrogenated state, that is, the carbon atoms at these positions are hydrogenated to form a saturated bond.
    "1H - pyrrolo [3,2 - c] pyridine", which is the core structure of the compound. Where "pyrrolo" refers to the pyrrole ring, and "pyridine" refers to the pyridine ring. The two are fused in a specific way, that is, the way represented by [3,2 - c]. Specifically, the pyrrole ring and the pyridine ring fuse with each other in a specific atomic connection to form a unique fused ring structure. 1H represents the hydrogen atom at position 1.
    Overall, this compound uses the pyrrolido-pyridine fused ring as the core, which is connected to the benzyl group at position 5, and is hydrogenated at positions 4, 5, 6, and 7, which together constitute its unique chemical structure. Its structure contains multiple carbon atoms and hydrogen atoms, and each atom is connected by a specific chemical bond to form a stable spatial configuration. This structure endows the compound with specific physical and chemical properties, and may have specific uses in organic synthesis, medicinal chemistry and other fields.
    What are the physical properties of 5-benzyl-4,5,6, 7-tetrahydro-1H-pyrrolo [3,2-c] pyridine
    5-Benzyl-4,5,6,7-tetrahydro-1H-pyrrolido [3,2-c] pyridine, which has many physical properties. Under normal conditions, it is solid, and its stability is quite good due to the molecular structure containing benzene ring and heterocyclic system.
    Looking at its melting point, it is in a specific temperature range, which is determined by the intermolecular force and the degree of structure compactness. And this substance exhibits a certain solubility in common organic solvents, soluble in organic solvents such as dichloromethane and chloroform, but has little solubility in water, which is caused by the difference between its molecular polarity and that of water. < Br >
    Then again, its density, due to the molecular structure and atomic weight, has a specific value and is in the macroscopic state of matter. As for its appearance, it is often white or white powder, which is related to the molecular aggregation morphology and crystal form.
    The physical properties of this object are determined by its unique molecular structure. The chemical bonds and spatial arrangement between atoms show the above physical properties in the macroscopic view, which are of great significance in chemical research and related application fields.
    What are the synthesis methods of 5-benzyl-4,5,6, 7-tetrahydro-1H-pyrrolo [3,2-c] pyridine
    To prepare 5-benzyl-4,5,6,7-tetrahydro-1H-pyrrolido [3,2-c] pyridine, there are several common synthesis methods. First, it can be made from suitable starting materials and reacted in multiple steps. First, take a compound containing a specific functional group, and under suitable reaction conditions, such as a catalyst and a specific temperature and pressure, cyclize the molecule to construct the basic skeleton of pyrrolido-pyridine. When the skeleton is initially formed, then introduce benzyl. When introducing benzyl, benzyl halide can be selected. Under the action of base, benzyl is connected to the target molecule through nucleophilic substitution reaction.
    Second, another type of compound is also used as the starting point, and the functional group is modified first to create an activity check point that is conducive to subsequent reactions. Then, the condensation reaction is used to splice different fragments and gradually build the molecular structure. During the reaction process, the reaction conditions, such as pH and temperature, need to be carefully regulated to ensure the selectivity and yield of each step of the reaction. After the approximate structure is formed, the tetrahydro part is hydrogenated to obtain 5-benzyl-4,5,6,7-tetrahydro-1H-pyrrolido [3,2-c] pyridine.
    Or, the strategy of biomimetic synthesis can be tried. Mimicking some biosynthetic pathways of such compounds in nature, with the help of enzymes or enzyme mimics, synthesis is achieved under milder conditions. Although this method is challenging, it may provide a greener and more efficient way for synthesis. However, no matter what method is used, the reaction conditions need to be carefully studied, and the purity and structure of the intermediate and product need to be accurately identified to ensure the success of the synthesis.
    In which fields is 5-benzyl-4,5,6, 7-tetrahydro-1H-pyrrolo [3,2-c] pyridine used?
    5-Benzyl-4,5,6,7-tetrahydro-1H-pyrrolido [3,2-c] pyridine is used in many fields such as medicine and materials.
    In the field of medicine, it has a unique chemical structure or can act on specific biological targets. After research, it has been found that the benzyl and tetrahydropyrrolido-pyridine parts of its structure may interact with certain proteins and enzymes in the human body. For example, in the development of drugs for neurological diseases, it may regulate neurotransmitter transmission and is expected to be used in the treatment of Parkinson's disease, Alzheimer's disease, etc. Because it can precisely bind to relevant targets, affect nerve cell signaling pathways and improve patient symptoms. In the exploration of anti-cancer drugs, it also has potential, which may inhibit the proliferation of tumor cells and induce their apoptosis, providing a new way to overcome cancer problems.
    In the field of materials, it can be used as an intermediate in organic synthesis. With its special structure, it can participate in the preparation of a variety of functional materials. For example, when preparing materials with photoelectric properties, the introduction of this compound can adjust the electron cloud distribution of the material, change its optical absorption and emission characteristics, and be used in the manufacture of organic Light Emitting Diodes (OLEDs), solar cells, etc. Because it can optimize material properties, improve device efficiency and stability, and promote the progress of materials science.
    In addition, in the research and development of pesticides, new pesticides may be designed based on their structure. Utilizing its ability to bind to specific receptors in organisms, high-efficiency, low-toxicity and environmentally friendly pesticides have been developed, which precisely act on pests and reduce the impact on the environment and non-target organisms, which is of great significance for the sustainable development of agriculture.
    What is the market outlook for 5-benzyl-4,5,6,7-tetrahydro-1H-pyrrolo [3,2-c] pyridine
    5-Benzyl-4,5,6,7-tetrahydro-1H-pyrrolido [3,2-c] pyridine has considerable market prospects in the world. Looking at the present, the field of pharmaceutical and chemical industry is developing rapidly, and many new drug research and development have a growing demand for characteristic heterocyclic compounds. As a unique nitrogen-containing heterocyclic structure, this compound has great potential in pharmaceutical research and development.
    It can be used as a key intermediate for the creation of new drugs. Nowadays, people pay more and more attention to health, and the pharmaceutical market continues to expand. The development of new drugs is an inevitable trend. Drugs developed on the basis of it may show good efficacy for specific diseases. In the field of anti-depressant and anti-anxiety drug research and development, it has been found that such structures can help optimize the combination of drugs with targets and improve drug efficacy, so the demand is expected to increase.
    Furthermore, in the field of organic synthetic chemistry, the unique structure of this compound provides a broad exploration space for organic synthetic chemists. Through various chemical transformations, more complex and unique organic molecules can be constructed to meet the needs of materials science and other fields. With the advancement of science and technology, materials science is eager for new functional materials. This compound may emerge in material synthesis and open up new application directions.
    However, although the market prospect is good, there are also challenges. The synthesis process needs to be continuously optimized to reduce costs and increase productivity in order to meet the large-scale demand of the market. And the road to new drug research and development is long, and rigorous clinical trials are required. Only by breaking through many tests can the potential of this compound in the field of medicine be fully released and occupy an important place in the market.