2-(4-Chloro-3-sulfamoylbenzoyl)benzoic acid

95%

Reagent Code: #163211
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CAS Number 5270-74-6

science Other reagents with same CAS 5270-74-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.75 g/mol
Formula C₁₄H₁₀ClNO₅S
badge Registry Numbers
MDL Number MFCD09753828
thermostat Physical Properties
Boiling Point 638.6 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.537 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of sulfa-based pharmaceuticals, particularly carbonic anhydrase inhibitors. It plays a key role in the production of diuretic drugs such as acetazolamide and methazolamide, which are used to treat glaucoma, epilepsy, and altitude sickness. Its structure allows for effective binding to carbonic anhydrase enzymes, making it valuable in designing drugs that regulate fluid balance and intraocular pressure. Also utilized in research for developing new sulfonamide derivatives with potential therapeutic effects.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,590.00
inventory 250mg
10-20 days ฿26,020.00
inventory 1g
10-20 days ฿50,580.00

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2-(4-Chloro-3-sulfamoylbenzoyl)benzoic acid
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Used primarily as an intermediate in the synthesis of sulfa-based pharmaceuticals, particularly carbonic anhydrase inhibitors. It plays a key role in the production of diuretic drugs such as acetazolamide and methazolamide, which are used to treat glaucoma, epilepsy, and altitude sickness. Its structure allows for effective binding to carbonic anhydrase enzymes, making it valuable in designing drugs that regulate fluid balance and intraocular pressure. Also utilized in research for developing new sulfona

Used primarily as an intermediate in the synthesis of sulfa-based pharmaceuticals, particularly carbonic anhydrase inhibitors. It plays a key role in the production of diuretic drugs such as acetazolamide and methazolamide, which are used to treat glaucoma, epilepsy, and altitude sickness. Its structure allows for effective binding to carbonic anhydrase enzymes, making it valuable in designing drugs that regulate fluid balance and intraocular pressure. Also utilized in research for developing new sulfonamide derivatives with potential therapeutic effects.

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