4-Chloro-3-sulfamoylbenzoic acid
98%
- Product Code: 119126
Alias:
4-Chloro-3-sulfonylaminobenzoic acid
CAS:
1205-30-7
Molecular Weight: | 235.64 g./mol | Molecular Formula: | C₇H₆ClNO₄S |
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EC Number: | MDL Number: | MFCD00012375 | |
Melting Point: | 256-258 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
4-Chloro-3-sulfamoylbenzoic acid is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of diuretic and antihypertensive drugs, particularly those targeting the inhibition of carbonic anhydrase enzymes. This compound is also utilized in research settings for the preparation of sulfonamide derivatives, which are explored for their potential therapeutic applications, including antimicrobial and anticancer properties. Additionally, it finds use in organic synthesis as a building block for creating more complex molecules with specific biological activities.
Product Specification:
Test | Specification |
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Melting Point | 258-263 |
Purity (HPLC) | 98-100 |
Appearance | White Or Off-White Powder |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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25.000 | 10-20 days | ฿1,000.00 |
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100.000 | 10-20 days | ฿2,050.00 |
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500.000 | 10-20 days | ฿9,260.00 |
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4-Chloro-3-sulfamoylbenzoic acid
4-Chloro-3-sulfamoylbenzoic acid is primarily used in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of diuretic and antihypertensive drugs, particularly those targeting the inhibition of carbonic anhydrase enzymes. This compound is also utilized in research settings for the preparation of sulfonamide derivatives, which are explored for their potential therapeutic applications, including antimicrobial and anticancer properties. Additionally, it finds use in organic synthesis as a building block for creating more complex molecules with specific biological activities.
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