2 Ethenyl 5 Methoxy 1h Pyrrolo 3 2 B Pyridine
pyridine pyrrole pyrazine piperidine piperazine

2-ethenyl-5-methoxy-1H-pyrrolo[3,2-b]pyridine

    Specifications

    HS Code

    989900

    Chemical Formula C10H10N2O
    Physical State Solid (predicted)
    Solubility In Water Low (predicted)
    Solubility In Organic Solvents Soluble in some organic solvents (predicted)
    Uv Vis Absorption Characteristic absorption bands in UV - Vis region (dependent on structure)
    Ir Absorption Characteristic absorption peaks related to functional groups
    Chemical Reactivity Can participate in reactions typical of pyrrolo[3,2 - b]pyridine and vinyl groups

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    General Information
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    Frequently Asked Questions

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    What is the chemical structure of 2-ethenyl-5-methoxy-1H-pyrrolo [3,2-b] pyridine?
    2-Vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine, this is an organic compound. The description of its structure needs to be viewed from each part one by one.
    "1H-pyrrolido [3,2-b] pyridine", this is the core parent ring structure. Pyridine is a nitrogen-containing six-membered heterocyclic ring with aromatic properties. Pyrrole and fused with it, pyrrole is a nitrogen-containing five-membered heterocyclic ring. Where the two rings are fused, according to specific numbering rules, this structure constructs a unique fused ring system.
    "2-vinyl", indicating that there is a vinyl (-CH = CH ³) attached at the second position of the core structure. Vinyl is unsaturated and adds an active reaction check point to the compound.
    "5-methoxy", meaning that methoxy (-OCH 🥰) is attached at the 5th position. Methoxy groups contain oxygen atoms and have certain electronic effects, which can affect the physical and chemical properties of molecules.
    Thus, the structure of 2-vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine is composed of a core fused ring and a substituent at a specific position, and each part interacts to give the compound its unique chemical behavior and properties.
    What are the physical properties of 2-ethenyl-5-methoxy-1H-pyrrolo [3,2-b] pyridine
    2-Vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine, which is an organic compound. Its physical properties are quite critical, and it is important in many fields such as chemical industry and materials.
    When it comes to its properties, it may be solid at room temperature and pressure, or white to pale yellow powder, which is caused by the arrangement and interaction of atoms in the molecular structure. The melting point of this compound is about a specific range, or due to intermolecular forces, it needs to reach a certain temperature before it can be melted into a liquid state.
    Its solubility also has characteristics, and it may have a certain solubility in organic solvents, such as ethanol, dichloromethane, etc. In the molecular structure of the Gain, some groups can interact with organic solvent molecules such as hydrogen bonds and van der Waals forces, so they can dissolve in them. However, in water, the solubility may be extremely low, and the hydrophobic part of the molecule accounts for a large proportion, making it difficult to form effective interactions with water molecules.
    In addition, the stability of the compound is also worthy of attention. Under normal environmental conditions, without the influence of special chemical reagents or extreme physical conditions, its structure may remain relatively stable. In case of high temperature, strong oxidizing agents or strong acids and bases, or chemical reactions may occur, resulting in structural changes. This stability is derived from the strength of the chemical bonds within the molecule and the stability of the spatial structure.
    From the above, it can be seen that the physical properties of 2-vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine, such as its properties, melting point, solubility and stability, are determined by its unique molecular structure. In practical applications, the grasp of these properties is crucial.
    What are the common uses of 2-ethenyl-5-methoxy-1H-pyrrolo [3,2-b] pyridine?
    2-Ethenyl-5-methoxy-1H-pyrrolo [3,2-b] pyridine is an organic compound that is very important in chemical research and related industrial practices. Its common uses are as follows:
    First, in the field of pharmaceutical chemistry, this compound is often an important intermediate in drug synthesis. Due to its unique molecular structure, it has specific chemical activity and spatial configuration, and can participate in various chemical reactions to construct complex drug molecular structures. Through ingenious chemical modification and reaction steps, it can be converted into drugs with specific pharmacological activities, or act on specific biological targets to treat various diseases. For example, in the development of anti-cancer drugs, its structural properties can be used to design drug molecules that combine with tumor cell targets, block tumor cell growth signaling pathways, and thus inhibit tumor growth.
    Second, in the field of materials science, this compound may be used as a synthetic raw material for functional materials. Due to its structure endowing certain electronic and optical properties, it can be used to prepare organic optoelectronic materials. For example, after specific processing, it can be applied to the field of organic Light Emitting Diode (OLED), which plays a key role in improving the luminous efficiency, stability and color purity of OLED devices; or it can be used to prepare organic solar cell materials to help improve the photoelectric conversion efficiency of solar cells.
    Third, in the basic research of organic synthetic chemistry, 2-ethenyl-5-methoxy-1H-pyrrolo [3,2-b] pyridine is often used as a model compound. By studying the chemical reaction mechanism and reaction condition optimization, chemists can deeply explore the laws and characteristics of organic reactions, provide theoretical basis and practical experience for the development of new organic synthesis methods and strategies, and promote the continuous development of organic synthetic chemistry.
    What are the synthesis methods of 2-ethenyl-5-methoxy-1H-pyrrolo [3,2-b] pyridine
    To prepare 2-vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine, there are many methods, each has its own advantages, choose the good one and follow it to get the best effect.
    First, it can be started by methoxy-containing pyridine derivatives. First, a suitable substituent is introduced into the pyridine structure to make the pyridine ring have a specific activity, which is a key step. Then, through a delicate reaction, the pyrrole ring is constructed to form a pyrrolido [3,2-b] pyridine skeleton. As for the introduction of vinyl, it can be achieved by a specific alkylation reaction after the pyrrolido-pyridine skeleton is formed. In this process, the choice of alkenylation reagents and the control of reaction conditions, such as temperature, solvent, catalyst, etc., all affect the yield and purity of the product.
    Second, pyrrole derivatives can also be used. First construct the basic structure of pyrrolido-pyridine, and then introduce methoxy groups through methoxylation to change the molecular electron cloud distribution and affect its chemical activity. Finally, vinyl is introduced in an appropriate way. In this step, the selectivity of the vinyl introduction position needs to be considered to ensure the target product.
    Third, the tandem reaction catalyzed by transition metals can be used. This is a relatively novel method that uses transition metals as the catalytic core to make multi-step reactions occur continuously in the same system. The construction of pyrrole and pyrrole rings and the introduction of methoxy and vinyl groups can be achieved simultaneously. However, this method requires extremely high activity and selectivity of catalysts, and the reaction mechanism is complex. Fine regulation of reaction parameters is required to effectively synthesize the target product.
    All these methods have advantages and disadvantages. In actual synthesis, it is necessary to weigh the availability of raw materials, ease of control of reaction conditions, cost-effectiveness and many other factors to choose the optimal path to obtain 2-vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine.
    2-ethenyl-5-methoxy-1H-pyrrolo [3,2-b] pyridine is used in which areas
    2-Vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine, although not widely known, is useful in specific scientific and industrial fields.
    In the field of pharmaceutical research and development, such nitrogen-containing heterocyclic compounds are often the key structural units for the creation of new drugs. Due to their unique chemical structure or diverse biological activities, they can be used as potential drug lead compounds. By modifying their structures, researchers may be able to develop innovative therapies for specific diseases, such as anti-tumor, anti-viral, anti-inflammatory drugs, to solve the suffering of the world's diseases.
    In the field of materials science, 2-vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine may exhibit unique optoelectronic properties. It can be used to prepare organic Light Emitting Diode (OLED), solar cells and other optoelectronic device materials, which contribute to improving device efficiency and performance. It may also play a role in the design and synthesis of organic semiconductor materials, promoting the development of electronic devices in the direction of lightness and efficiency.
    Furthermore, in the field of chemical synthesis, this compound can be used as an important intermediate and participate in the construction of complex organic molecules. Chemists use it as a starting material and use various chemical reactions to ingeniously build complex organic compounds, expand the boundaries of organic synthesis, and lay the material foundation for the research and development of new materials and new drugs.
    In summary, 2-vinyl-5-methoxy-1H-pyrrolido [3,2-b] pyridine has potential application value in the fields of medicine, materials and chemical synthesis, which needs to be further explored and excavated by researchers.