3 Sulfonyl Amino 2 Thiophene
quinoline thiophene imidazole thiazole

3-Sulfonyl amino-2-thiophene

Taiy Chemical

    Specifications

    HS Code

    241534

    Chemical Formula C₄H₄NO₂S₂
    Molar Mass 163.21 g/mol
    Appearance Typically solid
    Odor May have a characteristic sulfur - related odor
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
    Melting Point Specific melting point data would depend on isomers and purity
    Boiling Point Data varies based on purity and structural details
    Stability Can be stable under normal conditions but may react with strong oxidizing agents
    Reactivity Can participate in substitution reactions due to the presence of functional groups

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    General Information
    Where to Buy 3-Sulfonyl amino-2-thiophene in China?
    As a trusted 3-Sulfonyl amino-2-thiophene 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 3-Sulfonyl amino-2-thiophene 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 application fields of 3-Sulfonyl amino-2-thiophene?
    3-Sulfonylamino-2-thiophene is useful in many fields.
    In the field of medicinal chemistry, it can be said to be crucial. Because of its unique molecular structure, it can interact with specific targets in organisms. When doctors make pharmaceuticals, they can use it as a key raw material to synthesize compounds with unique pharmacological activities. Or it can be used to develop antibacterial drugs, which can inhibit the growth and reproduction of bacteria by interfering with the physiological metabolic pathway of bacteria, and help doctors fight bacterial infections. Or it can participate in the creation of anti-tumor drugs, providing new hope for conquering cancer by affecting the proliferation and apoptosis of tumor cells and other key processes.
    In the field of materials science, 3-sulfonylamino-2-thiophene is also promising. Material artisans can use its characteristics to develop new functional materials. For example, in the field of optoelectronic materials, it may improve the electrical conductivity and optical properties of materials. Integrating it into organic semiconductor materials is expected to improve the absorption and conversion efficiency of materials to light, and provide assistance for the manufacture of efficient solar cells, Light Emitting Diode and other optoelectronic devices, thereby promoting the progress of energy and lighting technology.
    Furthermore, in the field of organic synthetic chemistry, 3-sulfonylamino-2-thiophene can be regarded as a key synthetic building block. Organic synthesizers, with their special functional groups, can build more complex and diverse organic compounds through various chemical reactions. Using it as the starting material, through ingenious reaction design and step arrangement, organic molecules with unique structures and functions can be synthesized, which contributes to the development of organic chemistry and expands the variety and application range of organic compounds.
    What are the physical and chemical properties of 3-Sulfonyl amino-2-thiophene?
    3-Sulfonylamino-2-thiophene This substance has various physical and chemical properties. Its properties may be white to light yellow powder, and it is fine in appearance. In terms of solubility, it is slightly soluble in common water, but in some organic solvents, such as ethanol, acetone, etc., it can have a certain solubility. This is due to the characteristics of sulfonylamino and thiophene rings in the molecular structure. Sulfonylamino groups are polar, while thiophene rings have certain hydrophobicity. The interaction between the two causes their solubility to be so.
    When it comes to melting point, it is finely determined that it is within a certain temperature range. This melting point characteristic is its inherent physical property and is closely related to the force between molecules. The interaction between molecules, such as van der Waals forces and hydrogen bonds, determines the energy required for it to change from solid to liquid, that is, the melting point.
    Its chemical properties are also quite unique. Sulfonylamino sulfur atoms are in a high valence state and have certain oxidation properties. Under suitable reaction conditions, they can participate in many redox reactions. Thiophene rings are aromatic due to their conjugate structure and can undergo electrophilic substitution reactions, such as halogenation and nitrification. And the substituents on the ring will have a significant impact on the reaction activity and selectivity. The effects of ortho and para-substituents are different, which are all due to the combined effect of electronic effects and spatial effects. < Br >
    Because of its structure containing heteroatoms such as nitrogen and sulfur, it can form coordination compounds with metal ions, showing unique coordination chemical properties, which may have potential application value in catalysis, materials science and other fields. In short, the physical and chemical properties of 3-sulfonylamino-2-thiophene are rich and diverse, laying the foundation for its research and application in many fields.
    What are the synthesis methods of 3-Sulfonyl amino-2-thiophene?
    There are various ways to synthesize 3-sulfonylamino-2-thiophene. One method can be started from thiophene. First, the thiophene is sulfonated, and sulfuric acid or fuming sulfuric acid is used as the sulfonating agent. Under appropriate temperature, a sulfonic acid group can be introduced into the thiophene ring to obtain thiophenesulfonic acid. Then, by reacting with ammonia or amines, the sulfonic acid group can be converted into a sulfonamide group, and then 3-sulfonylamino-2-thiophene is obtained. During this process, when sulfonating, the temperature, reaction time and the amount of sulfonating agent must be carefully controlled to avoid excessive sulfonation or side reactions. < Br >
    There is another method, or it can start from thiophene derivatives containing suitable substituents. For example, if there is a 2-halothiophene, a sulfonate group can be introduced first, and then the sulfonate group can be converted into a sulfonamido group through reactions such as aminolysis, so as to obtain the target product. In this path, the selection of halothiophene, the activity of halogen atoms, and the optimization of aminolysis conditions are crucial to the success or failure of the synthesis.
    Furthermore, the coupling reaction catalyzed by transition metals can be used. The structure of 3-sulfonylamino-2-thiophene was constructed by coupling the appropriate thiophene-containing structural substrate and sulfonylamino precursor under the catalysis of transition metal catalysts such as palladium and copper. In this method, the type of catalyst, the choice of ligand, and the use of reaction solvent and base all affect the efficiency and selectivity of the reaction.
    In short, there are various methods for synthesizing 3-sulfonylamino-2-thiophene. Each method has its own advantages and disadvantages. The appropriate method should be carefully selected according to the actual situation, such as the availability of raw materials, the ease of control of reaction conditions, and the purity requirements of the target product.
    What is the price range of 3-Sulfonyl amino-2-thiophene in the market?
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    When looking for this manufacturer, you need to pay attention to many matters. First, safe production is essential. Chemical production is related to human life and the environment, and the selected manufacturer must abide by safety regulations and practice safe production. Second, product quality is of paramount importance. This substance may be used in special fields, and the manufacturer must meet Quality Standards before it can be used. Third, reputation and reputation should not be ignored. Manufacturers with good reputation may have more reliable products and services.
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