2 Amino 4 Chlorobenzothiazole
quinoline thiophene imidazole thiazole

2-Amino-4-chlorobenzothiazole

    Specifications

    HS Code

    568127

    Chemical Formula C7H5ClN2S
    Molecular Weight 184.64
    Appearance Solid
    Color Off - white to light yellow
    Odor Typical organic compound odor
    Melting Point 159 - 162 °C
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, chloroform
    Stability Stable under normal conditions
    Hazard Class Irritant (may cause eye, skin, and respiratory irritation)

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    General Information
    Where to Buy 2-Amino-4-chlorobenzothiazole in China?
    As a trusted 2-Amino-4-chlorobenzothiazole 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 2-Amino-4-chlorobenzothiazole 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-amino-4-chlorobenzothiazole?
    2-Amino-4-chlorobenzothiazole is a crucial intermediate in the field of organic synthesis and is widely used in many fields.
    In the field of medicine, it can be used as a key raw material for the synthesis of antibacterial, antiviral and anti-tumor drugs. For example, some new antibacterial drugs, with the help of the unique chemical structure of 2-amino-4-chlorobenzothiazole, can effectively inhibit the activity of specific bacterial enzymes, block bacterial metabolic pathways, and achieve antibacterial effect. In the development of antiviral drugs, this intermediate can also play an important role in the construction of compounds with high affinity with key viral proteins and inhibit viral replication.
    In the dye industry, 2-amino-4-chlorobenzothiazole can be used to prepare dyes with bright color and excellent fastness. Its structure endows the dye with a good conjugate system, which can enhance the absorption and emission of light, making the dye show rich and diverse colors. And the intermediate can introduce different substituents through chemical modification, thereby adjusting the solubility and light resistance of the dye to meet the needs of different textile materials and dyeing processes.
    In the field of pesticides, pesticides synthesized from this intermediate have the characteristics of high efficiency, low toxicity and environmental friendliness. It can precisely act on specific physiological targets of pests, interfere with physiological processes such as pest growth and reproduction, and effectively control pests. For example, some pesticides can inhibit the function of specific ion channels in the pest's nervous system, resulting in pest paralysis and death. At the same time, compared with traditional pesticides, such pesticides synthesized based on 2-amino-4-chlorobenzothiazole have a short residue period in the environment and have less impact on the ecological environment.
    In summary, 2-amino-4-chlorobenzothiazole, with its unique chemical structure and reactivity, plays an indispensable role in many fields such as medicine, dyes, and pesticides, and is of great significance to promote the development of related industries.
    What are the physical properties of 2-amino-4-chlorobenzothiazole?
    2-% hydroxy-4-methoxybenzofuranone, which is a genus of organic compounds. Its physical properties are particularly important and are related to many practical applications. Details are as follows:
    - ** Properties **: Usually in the state of white to light yellow crystalline powder, this appearance characteristic is crucial for the identification and preliminary cognition of the substance. Looking at its color state, its purity and basic characteristics can be initially judged.
    - ** Melting point **: The melting point of the compound is in a specific range, about [X] ° C. Melting point is the inherent physical property of a substance. By measuring the melting point, its purity can be verified. If the purity is high, the melting point is sensitive and consistent with the theoretical value; if it contains impurities, the melting point often decreases and the melting range becomes wider.
    - ** Solubility **: In organic solvents, such as ethanol, acetone, etc., show good solubility, but poor solubility in water. This property is crucial in the separation, purification and preparation of solutions. In organic synthesis, according to its solubility, a suitable solvent can be selected for the reaction to promote the smooth progress of the reaction.
    - ** Stability **: Under normal conditions, it has certain stability. However, when exposed to strong oxidizing agents, strong acids or strong bases, chemical reactions may occur, resulting in structural changes. This stability feature must be considered during storage and use. It should be avoided from contact with the above substances and stored in a suitable environment to prevent deterioration.
    - ** Odor **: Often has a weak special smell. Although the smell is not the main basis for identifying the substance, it has certain reference value in specific scenarios, such as product odor control or Environmental Impact Assessment.
    What are the synthesis methods of 2-amino-4-chlorobenzothiazole?
    To prepare 2-amino-4-chlorobenzothiazole, there are many methods, and the common synthesis paths are described in detail below.
    First, o-amino-thiophenol and chloroacetic acid are used as the starting materials. First, o-amino-thiophenol is reacted with chloroacetic acid in a basic environment. Bases such as sodium hydroxide can help the two combine to form corresponding intermediates. This intermediate structure contains the required basic structure, but further cyclization is required to form a benzothiazole ring. The cyclization step often requires heating and supplemented by suitable catalysts, such as some Lewis acid catalysts. After this treatment, the intramolecular rearrangement and cyclization result in the final 2-amino-4-chlorobenzothiazole. The raw materials of this route are easy to purchase, and the reaction conditions are relatively mild. It is commonly used in laboratory and industrial preparation.
    Second, starting from 2-nitro-4-chlorobenzoic acid. First, 2-nitro-4-chlorobenzoic acid is reduced to 2-amino-4-chlorobenzoic acid. The reduction method can be catalytic hydrogenation method, using palladium carbon as a catalyst, and hydrogen gas is introduced to realize the transformation of nitro to amino group. Subsequently, 2-amino-4-chlorobenzoic acid interacts with sulfurization reagents such as phosphorus pentasulfide. After sulfurization and cyclization, the sulfur atom reacts with a specific group in the molecule to form a thiazole ring, and then the target product is obtained. Although the steps in this process are slightly complicated, the reaction selectivity of each step is good and the purity of the product is also high.
    Third, 4-chloro-2-methoxyaniline is used as the starting material. Shilling 4-chloro-2-methoxyaniline reacts with thiocyanate to form the corresponding thiocyanate intermediate. This intermediate undergoes a series of reactions such as hydrolysis and cyclization. The hydrolysis process can be carried out under acidic or basic conditions. Cyclization requires specific reaction conditions to promote the formation of intramolecular rings, and finally forms 2-amino-4-chlorobenzothiazole. The raw material of this route is unique, and the reaction process also has its own characteristics, which provides a different idea for the synthesis of this compound. < Br >
    All these synthesis methods have their own advantages and disadvantages. In practical application, it is necessary to comprehensively consider many factors such as raw material cost, reaction conditions, product purity, etc., and choose the optimal method.
    What is the price of 2-amino-4-chlorobenzothiazole in the market?
    In today's market, the price of 2-amino-4-chlorobenzothiazole is quite difficult to determine. The price of the cover often changes with time and depends on many factors.
    The price of its raw materials is very important when it comes to the price of 2-amino-4-chlorobenzothiazole. If the raw materials are easy to obtain and abundant in production, the price may be flat; if the raw materials are rare, there are many seekers and few suppliers, the price will rise.
    Furthermore, the technique of making this is also the main reason. If the technique is refined and efficient, and the manpower and material resources expended are small, the price may be inexpensive; if the technique is clumsy and ineffective, time-consuming and consumes a lot of goods, the price will be high.
    Also, the demand of the market has a huge impact on the price. If this item is needed by various industries, and the demand is like a rush, and the supply is in short supply, the price will rise; if the demand is few, the goods are accumulated in abundance, and the supply exceeds the demand, the price will drop.
    And the decrees of the four parties also affect the price. Or there are differences in taxes and regulations prohibiting discussion, which can make the price fluctuate.
    With common sense, the price of this item at present is between tens and hundreds of dollars per catty. However, this is only an approximate number. If you want to know the exact price, you must visit the cities and consult the businesspeople, and observe the facts at that time before you can obtain it.
    What are the storage conditions for 2-amino-4-chlorobenzothiazole?
    The storage conditions of 2-% hydroxy-4-mercaptoimidazole are crucial to the maintenance of its quality and the preservation of its efficacy. Although the "Tiangong Kaiwu" does not directly describe the storage method of this material, according to the ancient people's principle of storage of drugs and various materials, it can be deduced roughly.
    Cover the storage of ordinary things, the first thing is the dryness and humidity of the environment. This 2-% hydroxy-4-mercaptoimidazole should be placed in a dry place. If it is in a humid place, it is prone to moisture. The tide may cause its properties to change, or cause chemical reactions, which will damage its inherent properties. Like ancient Tibetan medicine, it is mostly placed in pottery jars and wooden boxes, sealed and stored in highly dry places to prevent moisture erosion.
    The second discussion on the temperature section. It is not suitable to be exposed to the hot sun, high temperature is easy to cause 2-% hydroxy-4-mercaptoimidazole to decompose and other changes. When placed in a cool place, make it at a suitable temperature to ensure the stability of its chemical properties. If you hide tea in the past, it is often placed in cellars or cool rooms to avoid the heat of the sun. This is also the case.
    In addition, it is necessary to prevent it from mixing with foreign bodies. 2-% hydroxy-4-mercaptoimidazole should be stored separately to avoid contact with other chemicals and sundries to prevent mutual pollution and reaction. The ancient Tibetan pills were all stored in special containers in one place, and they should not be mixed with other things to prevent the variation of medicinal properties.
    And the storage place should be protected from dust. Dust or attached to 2% hydroxy-4-mercaptoimidazole, affecting its purity and quality. In ancient collections of books, they were still wrapped in a envelope and placed in a clean shelf to prevent dust from staining. This can also be a lesson for storing this thing.
    In short, the storage of 2% hydroxy-4-mercaptoimidazole should be selected in a dry, cool, clean and isolated place, so that it can maintain good quality for a certain period of time without losing its due effect.