2 Hydrazin 4 Methylbenzothiazole
quinoline thiophene imidazole thiazole

2-Hydrazin-4-Methylbenzothiazole

    Specifications

    HS Code

    520067

    Chemical Formula C9H11N3S
    Molecular Weight 193.27
    Appearance Solid (assumed, as no specific given)

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    General Information
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    Frequently Asked Questions

    As a leading 2-Hydrazin-4-Methylbenzothiazole 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 main uses of 2-Hydrazin-4-Methylbenzothiazole?
    2-Hydrazyl-4-methylbenzothiazole, this substance has a wide range of uses. In the field of medicine, it can be used as a key intermediate to help synthesize drugs with specific biological activities. Due to its unique structure, it can precisely bind to targets in vivo, or regulate physiological processes, or exert antibacterial, anti-inflammatory, and anti-tumor effects, opening up new avenues for disease treatment.
    In the field of materials science, 2-hydrazyl-4-methylbenzothiazole also has outstanding performance. It can participate in the creation of high-performance materials, like some functional polymers, by introducing specific functional groups to improve material stability, heat resistance and mechanical properties, making the material suitable for aerospace, electronics and other fields with strict performance requirements.
    In the field of organic synthetic chemistry, it is an extremely important building block for organic synthesis. With its own activity check point, through various chemical reactions, complex organic compounds are constructed, providing powerful tools for organic synthetic chemists to expand the diversity of molecular structures and promoting the continuous development of organic synthetic chemistry.
    What are the physical properties of 2-Hydrazin-4-Methylbenzothiazole?
    2-Hydrazinyl-4-methylbenzothiazole is one of the organic compounds. Its physical properties are quite unique.
    Looking at its properties, at room temperature, it is mostly in a solid state or a crystalline state. Due to the interaction between molecules, the molecules are arranged in an orderly manner and take the shape of a solid state.
    When it comes to the melting point, the interaction between the benzothiazole ring and the hydrazine group and methyl group in the molecular structure gives it a specific melting point value. This melting point is the critical temperature for the substance to change from solid to liquid state, which is of great significance for its identification and purification.
    In terms of solubility, it may have certain solubility in organic solvents such as ethanol and dichloromethane. Interactions such as van der Waals forces and hydrogen bonds can be formed between the Gein organic solvent and the molecule of the compound, making it soluble. However, in water, its solubility or poor, due to the hydrophobic part of its molecule, that is, the presence of benzothiazole ring and methyl group, makes it difficult to fully affinity with water molecules.
    Its density is also an important characteristic of physical properties, reflecting the degree of close packing of molecules, which is closely related to molecular mass and crystal structure.
    In addition, the color state of the compound may be colorless to light yellow, which is related to the transition of electrons in the molecule and the conjugation system. The specific structure makes the electrons absorb and emit light in a specific wavelength range, so it shows this color. < Br >
    All these physical properties are determined by their molecular structure, which is also the basis for their application in many fields.
    What are the chemical properties of 2-Hydrazin-4-Methylbenzothiazole?
    The chemical properties of 2-hydrazine-4-methylbenzothiazole are quite unique. It is basic, and the genase molecule contains nitrogen atoms, which can form salts with acids. And the lone pair of electrons of the nitrogen atom can participate in the reaction, showing nucleophilicity under specific conditions, and can react with halogenated hydrocarbons and other electrophilic reagents to form new chemical bonds.
    It has a certain degree of reductivity, which originates from the existence of hydrazine groups. The nitrogen-nitrogen bond and nitrogen-hydrogen bond in the hydrazine group are more active. When encountering strong oxidants, it is easy to be oxidized, and an oxidation reaction occurs to form corresponding oxidation products.
    In the field of organic synthesis, this compound is often used as an intermediate. Its benzothiazole ring has a certain rigidity and conjugate structure, providing a specific chemical environment for the reaction. With the activity of hydrazine group, complex organic molecular structures can be constructed through various reactions.
    In addition, the substance may have tautomerism under certain conditions. Due to the relative activity of hydrogen atoms of hydrazine group, or migration, the molecular structure changes, showing different chemical properties and reactivity. This tautomerism has a significant impact on the chemical reaction process and product structure it participates in.
    What are 2-Hydrazin-4-Methylbenzothiazole synthesis methods?
    The synthesis method of 2-hydrazino-4-methylbenzothiazole is particularly crucial, which is related to the preparation and application of this compound. The synthesis method follows a number of paths.
    First, 4-methylbenzothiazole is introduced into the hydrazine group through a specific reaction. First, 4-methylbenzothiazole is reacted with a suitable reagent to form an active intermediate, and then the intermediate is reacted with hydrazine compounds and reacted with nucleophilic substitution to obtain 2-hydrazino-4-methylbenzothiazole. This process requires careful control of the reaction conditions, such as temperature, solvent, reactant ratio, etc., to ensure the smooth progress of the reaction and the purity of the product.
    Second, or start from the basic raw materials to gradually construct the structure of benzothiazole ring and hydrazine group. Through a multi-step reaction, the molecular framework is built and specific functional groups are introduced in sequence. The basic structure containing sulfur, nitrogen and methyl is prepared first, and then the benzothiazole ring is formed by cyclization, and then the hydrazine group is introduced at a suitable check point. Although this approach has many steps, if the reaction conditions are properly controlled at each step, the target product can also be obtained.
    When synthesizing, many factors must be paid attention to. The choice of reaction solvent has a great impact on the reaction rate and selectivity. Some polar solvents may be beneficial to nucleophilic substitution reactions, rather than polar solvents or suitable for specific cyclization steps. Temperature control is also key. Different reaction stages may require different temperatures. Too high or too low temperatures can cause side reactions to occur or the reaction rate is too slow. And the purity and proportion of the reactants also affect the synthesis effect. Accurate measurement and high-quality raw materials are the guarantee of successful synthesis.
    2-Hydrazin-4-Methylbenzothiazole what are the precautions during use
    2-Hydrazyl-4-methylbenzothiazole is a rather special chemical substance, and many matters need to be paid attention to during use.
    Bear the brunt of it, and safety protection must not be ignored. This substance may be toxic and irritating to a certain extent. When contacting, it is necessary to wear suitable protective equipment, such as gloves, goggles, protective clothing, etc., to prevent it from contacting the skin and eyes. If it is accidentally touched, rinse with plenty of water as soon as possible, and seek medical attention according to the actual situation.
    Furthermore, storage conditions are crucial. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. It should also be stored separately from oxidants, acids, etc., and must not be mixed to prevent dangerous chemical reactions.
    When using, the operation must be precise and standardized. Strictly follow the established operating procedures and dosage requirements, and must not be changed at will. Due to its reactivity or special, improper operation, or cause the reaction to go out of control and cause accidents.
    And its waste disposal should not be underestimated. It needs to follow relevant environmental regulations, handle it properly, and do not discard it at will to avoid pollution to the environment.
    In addition, the ventilation facilities in the place of use must be complete to facilitate the timely discharge of volatile gaseous substances, reduce the concentration of harmful substances in the air, and protect the health of users.
    In short, when using 2-hydrazyl-4-methylbenzothiazole, the above things should be given high attention and must not be taken lightly, so as to ensure the safety of the use process.