Ethyl 2-methyl-2-(4-sulfamoylphenyl)propanoate

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Reagent Code: #116849
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CAS Number 374067-94-4

science Other reagents with same CAS 374067-94-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.33 g/mol
Formula C₁₂H₁₇NO₄S
badge Registry Numbers
MDL Number MFCD09952205
thermostat Physical Properties
Boiling Point 402.23°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.225g/cm3
Storage Room temperature, dry and sealed

description Product Description

Used primarily in the pharmaceutical industry, this compound serves as an intermediate in the synthesis of various sulfonamide-based drugs. Its structure is key in developing medications that target bacterial infections, leveraging the sulfamoyl group's antimicrobial properties. Additionally, it finds application in research settings for studying enzyme inhibition, particularly in pathways involving carbonic anhydrase, which is relevant for treating conditions like glaucoma and edema. Its ester group also makes it a candidate for further chemical modifications, enabling the creation of derivatives with potential therapeutic uses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,625.00
inventory 100mg
10-20 days ฿3,753.00
inventory 1g
10-20 days ฿14,058.00

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Ethyl 2-methyl-2-(4-sulfamoylphenyl)propanoate
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Used primarily in the pharmaceutical industry, this compound serves as an intermediate in the synthesis of various sulfonamide-based drugs. Its structure is key in developing medications that target bacterial infections, leveraging the sulfamoyl group's antimicrobial properties. Additionally, it finds application in research settings for studying enzyme inhibition, particularly in pathways involving carbonic anhydrase, which is relevant for treating conditions like glaucoma and edema. Its ester group als

Used primarily in the pharmaceutical industry, this compound serves as an intermediate in the synthesis of various sulfonamide-based drugs. Its structure is key in developing medications that target bacterial infections, leveraging the sulfamoyl group's antimicrobial properties. Additionally, it finds application in research settings for studying enzyme inhibition, particularly in pathways involving carbonic anhydrase, which is relevant for treating conditions like glaucoma and edema. Its ester group also makes it a candidate for further chemical modifications, enabling the creation of derivatives with potential therapeutic uses.

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