Ethyl 2 Amino 4 5 6 7 Tetrahydro 1 3 Benzothiazole 4 Carboxylate
quinoline thiophene imidazole thiazole

ethyl 2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylate

    Specifications

    HS Code

    735785

    Chemical Formula C12H16N2O2S
    Molecular Weight 252.33 g/mol
    Appearance Typically a solid (description may vary)
    Melting Point Data specific to the compound (if available)
    Boiling Point Data specific to the compound (if available)
    Solubility In Water Limited to low solubility (general expectation, data may vary)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone (general behavior, data may vary)
    Density Data specific to the compound (if available)
    Pka Value Data specific to the amino group in the molecule (if available)
    Stability Stable under normal conditions, may decompose on heating or in presence of strong acids/bases

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    General Information
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    Frequently Asked Questions

    As a leading ethyl 2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylate 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 ethyl 2 - amino - 4,5,6,7 - tetrahydro - 1,3 - benzothiazole - 4 - carboxylate
    Ethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylic acid ester, an organic compound. Its chemical structure consists of several parts:
    -ethyl part, namely $C_ {2} H_ {5} - $, is a simple alkyl group with specific chemical activity and steric resistance effect, which often affects the physical and chemical properties of the compound, such as solubility and volatility. < Br > -2-amino, refers to the amino group ($- NH_ {2} $) connected to the benzothiazole ring at position 2, the amino group is basic and can participate in many chemical reactions, such as salting with acids, or participating in nucleophilic substitution reactions.
    -4,5,6,7-tetrahydro-1,3-benzothiazole core structure, which is formed by fusing the benzene ring with the thiazole ring, and the thiazole ring at positions 4, 5, 6, and 7 are saturated hydrogen atoms, endowing the structure with unique stability and electron cloud distribution, which affects the chemical reactivity and biological activity of the entire molecule. < Br > - 4-carboxylic acid ethyl ester, that is, $- COOCH_ {2} CH_ {3} $connected to the benzothiazole ring at position 4, the ester group is hydrolytic, and can undergo hydrolysis reaction under acid-base conditions to generate corresponding carboxylic acids and alcohols.
    The interaction of various parts of this compound structure determines its physical and chemical properties and chemical reactivity, and may have important application value in organic synthesis, pharmaceutical chemistry and other fields.
    What are the main uses of ethyl 2 - amino - 4,5,6,7 - tetrahydro - 1,3 - benzothiazole - 4 - carboxylate
    Ethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylic acid ester, which has a wide range of uses. In the field of medicine, it can be used as a key intermediate to create drugs for the treatment of various diseases. Due to its unique chemical structure, it can interact with specific targets in organisms, which has potential significance for the treatment of certain diseases, or can help develop new therapeutic methods and bring good news to patients.
    In the field of materials science, this compound may participate in the synthesis of materials with special properties. Due to the unique physical and chemical properties endowed by its structure, it can optimize some properties of materials, such as stability, optical properties, etc., and then be applied to many frontier fields such as electronics and optics, promoting the development of related industries.
    In agriculture, it can be used as a raw material to prepare agricultural chemicals, such as fungicides, insecticides, etc. With its chemical properties, it may have a good control effect on crop diseases and pests, helping agricultural harvest and ensuring food security.
    In scientific research and exploration, as an important chemical reagent, researchers can expand the knowledge boundary of organic synthesis chemistry by studying its reaction properties and structural modifications, providing opportunities for the development of new reactions and new methods, and promoting the continuous progress of chemistry.
    What is the synthesis method of ethyl 2 - amino - 4,5,6,7 - tetrahydro - 1,3 - benzothiazole - 4 - carboxylate
    There are currently methods for preparing ethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylate, which are described in detail below.
    First take the appropriate starting material, usually based on sulfur and nitrogen compounds. For example, select a specific aniline derivative and a sulfur-containing carbonyl compound, the two need to be mixed according to a certain stoichiometric ratio. In the reaction vessel, add an appropriate amount of solvent, such as ethanol, dichloromethane and other organic solvents, whose function is to uniformly disperse the reactants and promote the smooth progress of the reaction.
    Then, add an appropriate amount of catalyst to the reaction system. The choice of this catalyst depends on the reaction rate and yield. Common acid or base catalysts can be considered, depending on the characteristics of the reactants. Heat the reaction system to maintain a suitable temperature range, or between 50 and 100 degrees Celsius. This temperature range can effectively promote the reaction without excessive decomposition of the reactants.
    During the heating and stirring process, the reactant molecules collide and react with each other. After complex chemical changes, the target product ethyl - 2 - amino - 4, 5, 6, 7 - tetrahydro - 1, 3 - benzothiazole - 4 - carboxylate is gradually formed. After the reaction is completed, the pure product is usually obtained from the reaction mixed system by extraction, distillation, column chromatography and other separation and purification methods. Extraction can separate the product by the difference in solubility of different solvents to the product and impurities; distillation can separate the product from impurities according to different boiling points; column chromatography can take advantage of the different adsorption capacity of adsorbents to different substances to achieve the purpose of purification. After these steps, pure ethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylate can be obtained.
    What are the physical properties of ethyl 2 - amino - 4,5,6,7 - tetrahydro - 1,3 - benzothiazole - 4 - carboxylate
    Ethyl 2 - amino - 4,5,6,7 - tetrahydro - 1,3 - benzothiazole - 4 - carboxylate (2 - amino - 4,5,6,7 - tetrahydro - 1,3 - benzothiazole - ethyl 4 - carboxylate), the physical properties are as follows:
    Its shape or white to off-white crystalline powder is fine in appearance and smooth to the touch. The melting point is about a specific range, and may vary slightly depending on the preparation process and purity, but it is roughly between [X] ° C and [X] ° C. The determination of the melting point is the key indicator to determine its purity and characteristics.
    In terms of solubility, this substance can be dissolved in organic solvents such as ethanol and acetone to a certain extent. In ethanol, with the rise of temperature, the solubility gradually increases, showing the appearance of hot dissolution and cold precipitation; however, in water, its solubility is not good, and it is difficult to form a uniform dispersion state. This difference in solubility is due to the fact that there are both organic groups and hydrophobic parts in its molecular structure.
    In terms of stability, in a dry environment at room temperature, it can be stored for a long time and its properties are less changed; in case of strong acid and alkali, its structure may be damaged and hydrolysis and other reactions occur. Under light, there will also be slow decomposition and gradual change in color, so it needs to be protected from light and dry storage to ensure its quality. < Br >
    Its density is about [X] g/cm ³, reflecting the compactness of its molecules. In addition, its refractive index also has specific values, and under specific wavelengths of light, it can exhibit unique optical properties, which are also significant for identification and purity analysis.
    The above physical properties are key guidelines for its synthesis, preparation and application, and are related to the control of reaction conditions, the choice of dosage forms and the determination of applicable scenarios.
    Ethyl 2 - amino - 4,5,6,7 - tetrahydro - 1,3 - benzothiazole - 4 - carboxylate
    Fuethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylic acid ester. The discussion of the market prospect of this compound is quite complex and diverse.
    Looking at its use, this compound may have potential applications in the field of medicinal chemistry. Geiinbenzothiazole structures are often key parts of many drug molecules and can participate in the action of specific biological targets. If based on them, new antibacterial, anti-inflammatory, or even anti-tumor drugs may be developed. In the pharmaceutical market, if such innovative compounds can demonstrate good biological activity and safety, they will surely attract the attention of pharmaceutical companies, and the market prospect may be quite promising.
    In the field of agricultural chemistry, such compounds may be used to create new pesticides. Benzothiazole derivatives often have certain bactericidal and insecticidal activities. If ethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylate has been proven to have this effect and is environmentally friendly and has low residues, it is expected to occupy a place in the pesticide market to meet the needs of modern agriculture for efficient and environmentally friendly pesticides.
    However, its marketing activities also pose challenges. If the process of synthesizing the compound is complex and expensive, its large-scale production and application will be limited. And in the process of developing new drugs or new pesticides, it needs to go through rigorous tests and approvals, which takes a long time and requires huge investment. If it cannot pass smoothly, the previous efforts may be in vain.
    Furthermore, market competition is also a factor that cannot be ignored. Compounds of the same type or with similar efficacy may have entered the market first and occupy a certain share. To make ethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylic acid ester stand out, it is necessary to demonstrate unique advantages in performance and price.
    To sum up, the market prospect of ethyl-2-amino-4,5,6,7-tetrahydro-1,3-benzothiazole-4-carboxylic acid ester, although there are opportunities, there are also many challenges. It is necessary to comprehensively consider various factors such as R & D, production, and market in order to have a more accurate judgment on its prospects.