3 2 Fluorophenyl Imidazo 1 5 A Pyridine 1 Carbaldehyde
pyridine pyrrole pyrazine piperidine piperazine

3-(2-fluorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde

    Specifications

    HS Code

    522905

    Chemical Formula C15H10FN3O
    Molecular Weight 267.26 g/mol
    Appearance Solid (usually a powder, appearance can vary based on purity and synthesis method)
    Melting Point Data may vary depending on purity, typically needs experimental determination
    Boiling Point No common data available, difficult to measure due to potential decomposition before boiling
    Solubility In Water Low solubility, organic - soluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc.
    Pka No common data available, requires experimental determination as it depends on the acidity or basicity of the functional groups in the molecule
    Uv Vis Absorption Absorption bands in the ultraviolet - visible region, exact values depend on the electronic structure of the molecule
    Ir Absorption Characteristic absorption bands corresponding to functional groups such as C - H, C = N, C = O, C - F, etc., specific values for each group

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    General Information
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    Frequently Asked Questions

    As a leading 3-(2-fluorophenyl)imidazo[1,5-a]pyridine-1-carbaldehyde 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- (2-fluorophenyl) imidazo [1,5-a] pyridine-1-carbaldehyde
    3- (2-fluorophenyl) imidazolo [1,5-a] pyridine-1-formaldehyde, this is an organic compound. Its chemical properties are unique and worth exploring.
    First of all, its physical appearance is often a crystalline solid, with white or nearly colorless color, which is quite stable under normal conditions. Its melting point and boiling point are important physical constants. The melting point depends on the force between molecules, and the boiling point is related to the energy required for the molecule to break free from the liquid phase. The two are of great significance for its separation and purification.
    Solubility is also a key property. In organic solvents, such as dichloromethane and chloroform, it exhibits a certain solubility, which is convenient for acting as a reactant or product in organic synthesis reactions, which is conducive to uniform mixing of the reaction system and accelerates the reaction process. In water, its solubility is poor, due to the dominance of the hydrophobic part of the molecular structure.
    In terms of chemical activity, aldehyde groups are active functional groups and can participate in many reactions. Oxidation reactions can occur. Under the action of suitable oxidants, aldehyde groups can be converted into carboxyl groups, resulting in the derivation of a series of new compounds. It can also participate in reduction reactions, and aldehyde groups are reduced to alcohol hydroxyl groups, expanding the path for organic synthesis. At the same time, condensation reactions can be carried out with active hydrogen-containing compounds, such as with amines to form imines, which are not uncommon in the construction of complex organic molecular structures.
    In addition, the structure of benzene ring and imidazolopyridine endows the molecule with a certain conjugate system, which affects its electron cloud distribution, so that the molecule has specific optical properties and electron transfer ability, and may have potential applications in the field of materials science, such as in optoelectronic materials, or exhibit unique photophysical properties.
    What is the synthesis method of 3- (2-fluorophenyl) imidazo [1,5-a] pyridine-1-carbaldehyde
    To prepare 3- (2-fluorophenyl) imidazolo [1,5-a] pyridine-1-formaldehyde, the method is as follows:
    First take 2-fluorophenylacetonitrile, an appropriate amount of pyridine and potassium carbonate, place them in the reaction kettle, stir well. Slowly add an appropriate amount of ethyl bromoacetate, heat it to a moderate temperature, maintain this temperature, so that the two can fully react to generate the corresponding intermediate. This step requires careful temperature control and always pay attention to the reaction process to prevent side reactions from occurring.
    After the reaction is completed, the intermediate is purified by conventional separation methods, such as extraction, distillation, etc.
    Then, the purified intermediate is mixed with specific reagents (such as triethyl orthoformate, acetic anhydride, etc.), an appropriate amount of catalyst is added, and then heated to a certain extent. Continuous stirring is used to promote the cyclization reaction to generate 3- (2-fluorophenyl) imidazolo [1,5-a] pyridine. In this cyclization reaction step, the control of temperature and reaction time is crucial, which is related to the purity and yield of the product.
    Finally, the resulting 3- (2-fluorophenyl) imidazolo [1,5-a] pyridine is formylated. Take it and suitable formylating reagents (such as N, N-dimethylformamide, phosphorus oxychloride, etc.), and react under suitable conditions. After the reaction is completed, it is carefully purified through a series of post-processing operations, such as neutralization, extraction, column chromatography, etc., and finally obtain the target product 3- (2-fluorophenyl) imidazolo [1,5-a] pyridine-1-formaldehyde.
    Each step of the reaction requires precise control of the reaction conditions, strict requirements on the purity and dosage of raw materials, and the post-treatment process cannot be ignored, so that high purity and high yield products can be obtained.
    What is the main use of 3- (2-fluorophenyl) imidazo [1,5-a] pyridine-1-carbaldehyde
    3- (2-fluorophenyl) imidazolo [1,5-a] pyridine-1-formaldehyde, which has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of new drugs. Due to its unique molecular structure, it can interact with specific targets in organisms, helping to develop drugs with high selectivity and potency, or precise effect on specific disease mechanisms. For example, in the development of anti-cancer drugs, the structure of this compound can be modified, or new drugs with inhibitory effects on cancer cell growth and proliferation can be obtained.
    In the field of materials science, it may be able to participate in the synthesis of organic optoelectronic materials. Due to its structure imparting certain photoelectric properties, it can be reasonably designed to be combined with other materials to fabricate organic Light Emitting Diodes (OLEDs), solar cells and other devices to improve device performance and efficiency.
    In the field of organic synthetic chemistry, as an important synthetic building block, complex organic molecular structures can be constructed through various chemical reactions. With its unique functional groups and reactivity, nucleophilic addition and substitution reactions with different reagents provide organic synthetic chemists with various strategies to create organic compounds with novel structures and specific functions.
    What is the market price of 3- (2-fluorophenyl) imidazo [1,5-a] pyridine-1-carbaldehyde
    I do not know the market value of 3- (2-fluorophenyl) imidazolo [1,5-a] pyridine-1-formaldehyde. This compound was not published in Tiangong Kaiwu, because at the time of the publication of Tiangong Kaiwu, the research on such chemicals has not yet emerged. In today's chemical field, the price of such fine chemicals often varies due to a variety of factors. The difficulty of its preparation is one of the key factors. If the synthesis steps are complicated, the required raw materials are rare or the reaction conditions are harsh, the cost will be high and the price will rise accordingly. Furthermore, the market supply and demand conditions also affect its price. If there are many applicants and there are few suppliers, the price will rise; conversely, if the supply is sufficient and the demand is low, the price may fall. In addition, the price set by different manufacturers will also vary due to differences in technical level and production cost. To know the exact market price, you can obtain more accurate price information by checking the chemical product trading platform or inquiring the relevant chemical raw material suppliers.
    Precautions for storage and transportation of 3- (2-fluorophenyl) imidazo [1,5-a] pyridine-1-carbaldehyde
    For 3 - (2 - fluorophenyl) imidazolo [1,5 - a] pyridine-1 - formaldehyde, many matters need to be paid attention to during storage and transportation.
    Its nature or more active, when storing, the temperature and humidity of the first environment. It should be placed in a cool and dry place, protected from high temperature and humidity. High temperature can easily cause its chemical properties to change and accelerate deterioration; moisture may cause reactions such as hydrolysis, which will damage its purity.
    Furthermore, this material is sensitive to light or sensitive, so it should be stored away from light. It can be stored in a container that is opaque to light, or stored in a dark place to prevent light from causing it to decompose or photochemical reactions.
    During transportation, it is essential to maintain stability. It is necessary to ensure that the packaging is tight to prevent package damage and material leakage due to vibration and collision. Choose suitable packaging materials, such as chemical resistant materials, to avoid reaction with packaging materials.
    At the same time, follow relevant transportation regulations and standards, classify transportation according to its chemical properties, and isolate it from contraindicated substances. It is not allowed to be mixed. Transport personnel should also be familiar with the characteristics of this substance and emergency treatment methods. In case of emergencies, they can respond in time to ensure transportation safety. In this way, 3 - (2-fluorophenyl) imidazolo [1,5-a] pyridine-1-formaldehyde must be properly stored and transported to protect its quality and safety.