3-(N-(4-Chloro-3-methylisoxazol-5-yl)sulfamoyl)thiophene-2-carboxylic acid

97%

Reagent Code: #218172
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CAS Number 184040-74-2

science Other reagents with same CAS 184040-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.75 g/mol
Formula C₉H₇ClN₂O₅S₂
badge Registry Numbers
MDL Number MFCD18642943
thermostat Physical Properties
Boiling Point 556.983°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as an intermediate in the synthesis of sulfa drugs, particularly in the production of antimicrobial and anti-inflammatory agents. Its structure supports the development of compounds with enhanced binding affinity to bacterial enzymes, making it valuable in pharmaceutical research. Also utilized in agrochemicals for developing herbicides due to its stability and reactivity in sulfonamide formation. Commonly employed in medicinal chemistry for designing carbonic anhydrase inhibitors, which have applications in treating glaucoma and epilepsy.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,220.00
inventory 250mg
10-20 days ฿12,330.00
inventory 1g
10-20 days ฿30,750.00
3-(N-(4-Chloro-3-methylisoxazol-5-yl)sulfamoyl)thiophene-2-carboxylic acid
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Used as an intermediate in the synthesis of sulfa drugs, particularly in the production of antimicrobial and anti-inflammatory agents. Its structure supports the development of compounds with enhanced binding affinity to bacterial enzymes, making it valuable in pharmaceutical research. Also utilized in agrochemicals for developing herbicides due to its stability and reactivity in sulfonamide formation. Commonly employed in medicinal chemistry for designing carbonic anhydrase inhibitors, which have applic

Used as an intermediate in the synthesis of sulfa drugs, particularly in the production of antimicrobial and anti-inflammatory agents. Its structure supports the development of compounds with enhanced binding affinity to bacterial enzymes, making it valuable in pharmaceutical research. Also utilized in agrochemicals for developing herbicides due to its stability and reactivity in sulfonamide formation. Commonly employed in medicinal chemistry for designing carbonic anhydrase inhibitors, which have applications in treating glaucoma and epilepsy.

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