Benzenesulfonamide
98%
- Product Code: 123200
Alias:
Benzenesulfonamide
CAS:
98-10-2
Molecular Weight: | 157.19 g./mol | Molecular Formula: | C₆H₇O₂NS |
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EC Number: | 202-637-1 | MDL Number: | MFCD00007930 |
Melting Point: | 149-152 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
Benzenesulfonamide is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various sulfa drugs, which are effective antibiotics for treating bacterial infections. It also serves as a building block in the production of diuretics and antidiabetic medications. In addition, it finds application in organic chemistry as a reagent for protecting amines during chemical reactions. Its derivatives are utilized in the development of dyes, agrochemicals, and corrosion inhibitors. Furthermore, it plays a role in research as a model compound for studying sulfonamide-based interactions and mechanisms.
Product Specification:
Test | Specification |
---|---|
Melting Point | 151-154 |
Purity (HPLC) | 98-100 |
Appearance | White To Off-White Powder, Needles And/Or Chunks |
Infrared Spectrum | Conforms To Structure |
Solubility In Methanol | Almost Transparency, 25Mg/Ml (2.5%) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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100.000 | 10-20 days | ฿580.00 |
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500.000 | 10-20 days | ฿1,950.00 |
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1000.000 | 10-20 days | ฿3,180.00 |
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5000.000 | 10-20 days | ฿11,400.00 |
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Benzenesulfonamide
Benzenesulfonamide is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various sulfa drugs, which are effective antibiotics for treating bacterial infections. It also serves as a building block in the production of diuretics and antidiabetic medications. In addition, it finds application in organic chemistry as a reagent for protecting amines during chemical reactions. Its derivatives are utilized in the development of dyes, agrochemicals, and corrosion inhibitors. Furthermore, it plays a role in research as a model compound for studying sulfonamide-based interactions and mechanisms.
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