1 3 Benzothiazole 5 Carboxylic Acid
quinoline thiophene imidazole thiazole

1,3-Benzothiazole-5-carboxylic acid

    Specifications

    HS Code

    439648

    Name 1,3-Benzothiazole-5-carboxylic acid
    Molecular Formula C8H5NO2S
    Molecular Weight 179.196 g/mol
    Appearance Solid (likely powder or crystalline)
    Melting Point data needed
    Boiling Point data needed
    Solubility In Water data needed
    Solubility In Organic Solvents data needed
    Pka Value data needed
    Density data needed
    Flash Point data needed
    Hazard Class data needed

    As an accredited 1,3-Benzothiazole-5-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Storage
    Shipping
    Free Quote

    Competitive 1,3-Benzothiazole-5-carboxylic acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to info@alchemist-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: info@alchemist-chem.com

    General Information
    Where to Buy 1,3-Benzothiazole-5-carboxylic acid in China?
    As a trusted 1,3-Benzothiazole-5-carboxylic acid manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 1,3-Benzothiazole-5-carboxylic acid 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 1,3-benzothiazole-5-carboxylic acid?
    1,3-Benzodiazole-5-carboxylic acid is an organic compound. Its chemical properties are unique and have the following characteristics:
    - ** Acidic **: This compound contains a carboxyl group (-COOH), and the hydrogen atoms in the carboxyl group are easier to dissociate and exhibit acidity. In aqueous solution, it can react with bases to form corresponding carboxylic salts and water. For example, when reacted with sodium hydroxide (NaOH), 1,3-benzodiazole-5-carboxylate sodium and water will be formed, which is a typical acid-base neutralization reaction.
    - ** Esterification Reaction **: Carboxylic groups can be esterified with alcohols under acid-catalyzed conditions. If 1,3-benzodiazole-5-carboxylic acid and ethanol are catalyzed by concentrated sulfuric acid and heated, 1,3-benzodiazole-5-carboxylic acid ethyl ester and water will be formed. This reaction is often used in organic synthesis to prepare esters, many of which have special flavors and can be used in fragrances and other fields.
    - ** Nucleophilic Substitution Reaction **: Nucleophilic substitution reactions may occur at some positions on the 1,3-benzodiazole ring. Because the benzodiazole ring has a certain electron cloud density distribution, nucleophiles may attack suitable positions on the ring, thereby triggering substitution reactions. For example, nucleophiles attack the carbon atom adjacent to the nitrogen atom on the ring, causing the atom or group at this position to be replaced. This reaction mechanism is crucial in building more complex organic molecular structures.
    - ** Stability **: The structure of the 1,3-benzodiazole ring is relatively stable, which allows the compound to exist stably under general conditions. However, under severe conditions such as some specific strong oxidants or high temperatures, its structure may be damaged. During organic synthesis and storage, suitable reaction conditions and storage environments need to be selected according to their stability characteristics.
    What are the main uses of 1,3-benzothiazole-5-carboxylic acid?
    1,3-Benzodiazole-5-carboxylic acid, which has a wide range of uses. In the field of medicine, it is often used as a key intermediate to help synthesize a variety of specific drugs. For example, some compounds with specific pharmacological activities can build key molecular structures, laying the foundation for the development of new drugs for the treatment of difficult diseases, and playing an important role in the development of anti-cancer and antiviral drugs.
    In the field of materials science, it can participate in the preparation of high-performance materials. Like preparing polymer materials with special optical and electrical properties, introducing it into the polymer skeleton can effectively improve material stability, mechanical properties and processing properties. Take the high-performance composite materials used in the aerospace field as an example, its application can improve the comprehensive properties of materials and meet the demands of harsh environments.
    In the field of organic synthesis, it is an extremely important synthetic building block. With its unique chemical structure, it can react with many reagents to build complex organic molecular structures. Organic synthesis chemists often use its reactivity to design synthesis routes to achieve efficient synthesis of target products, providing key support for the creation and research of new compounds.
    In short, 1,3-benzodiazole-5-carboxylic acids have important uses in many fields such as medicine, materials, and organic synthesis, and are of great significance in promoting the development of related fields.
    What are the synthesis methods of 1,3-benzothiazole-5-carboxylic acid?
    The synthesis method of 1% 2C3-benzodiazine-5-carboxylic acid is related to the delicate skills in the field of organic chemistry. The following are common synthesis paths:
    First, phenols, aldodes and primary amines are used as starting materials and are formed by condensation reaction. This reaction condition is quite critical, and temperature, solvent and catalyst are all affected. Generally speaking, at a suitable temperature, a specific organic solvent is used as the medium, and an appropriate amount of catalyst is added. Phenol and aldehyde are condensed first, and then further reacted with primary amines to gradually construct benzodiazine rings, and finally carboxyl groups are introduced. For example, phenol, formaldehyde and p-aminobenzoic acid are selected in ethanol solvent, a small amount of acid is used as a catalyst, and the reaction is stirred at a certain temperature. After multi-step conversion, the target product can be obtained.
    Second, with the help of cyclization reaction strategy. First prepare an intermediate containing a specific functional group, and form a benzoxazine structure through an intramolecular cyclization reaction, and then introduce a carboxyl group in a suitable step. For example, compounds with alkenyl groups and phenolic hydroxyl groups are first synthesized, and the benzoxazine skeleton is constructed by intracellular nucleophilic cyclization, and then the carboxyl group is introduced at a suitable position through oxidation and substitution reactions. This process requires precise control of the reaction conditions to ensure the accuracy of the introduction of cyclization and carboxyl groups.
    Third, the metal-catalyzed Some metal catalysts can effectively promote the formation and carboxylation of benzodiazine rings. Metal complexes such as palladium and copper are used as catalysts to design suitable substrates to make the benzene ring and groups containing nitrogen and oxygen atoms cyclize under metal catalysis. At the same time, carboxyl groups are introduced at appropriate stages through suitable carboxylation reagents, such as carbon dioxide and carboxylic acid derivatives. This method requires high purity of the reaction system, catalyst dosage and reaction conditions, but it can provide an efficient and selective synthesis path.
    All kinds of synthetic methods have their own advantages and disadvantages. In practical application, it is necessary to comprehensively consider factors such as the availability of raw materials, the controllability of reaction conditions, the purity and yield of the product, and carefully select the appropriate synthetic method to achieve the purpose of efficient preparation of 1% 2C3-benzoxazine-5-carboxylic acid.
    What is the price of 1,3-benzothiazole-5-carboxylic acid in the market?
    At present, the price of 1,3-naphthalimidazole-5-carboxylic acid in the market has changed for many reasons.
    The production of this product, the price of raw materials, and the progress of technology all have a great impact on its price. If there is a shortage of raw materials, the price will be high; if new technologies are released, the cost of production can be reduced, and the price may be reduced.
    The demand of the market is also the key. In fields such as medicine and optoelectronics, if the demand for this product is prosperous, the price may rise; conversely, if the price is low, the price may be depressed.
    And the dispute between the industry also affects its price. Many merchants compete in the market, or adjust the price to occupy the market.
    As for the exact price at present, it is difficult to determine. However, if you want to know more about it, you can visit the market of chemical materials, consult the franchised merchants, or observe the price movement in the online business area. You can also read the industry report and the research report of the market to understand the state and change of its price. In this way, the price of 1,3-naphthalimidazole-5-carboxylic acid can be known more accurately in the market.
    What are the storage conditions for 1,3-benzothiazole-5-carboxylic acid?
    The storage conditions of 1% 2C3 - guangbindi incense - 5 - peony should be placed in a cool and dry place, and it should be protected from moisture and moisture, insects and moths.
    Fuguangbindi incense - 5 - peony, delicate, easy to be invaded by moisture and insects. If it is in a humid place, it is easy to cause its mildew and rot, and damage its medicinal effect; if it is eaten by insects, it will also greatly reduce the medicinal power and make it unusable. Therefore, when storing, it is very important to choose a cool and dry place.
    Shade, so that the properties of the medicine will not dissipate due to heat; dry, can eliminate the damage of moisture. And it needs to be checked frequently. If you see any traces of worms, you should quickly remove them in an appropriate way, or hide them with natural insect repellents such as prickly ash, or dry them in a well-ventilated and well-ventilated manner, but when drying, you also need to avoid the hot sun and avoid the essence of medicine. In this way, it is necessary to properly store Xiongbindi-5-peony, so that its medicinal power can last for emergencies.