n-Methyl-3-(trifluoromethyl)benzenesulfonamide

≥95%

Reagent Code: #214347
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CAS Number 882423-09-8

science Other reagents with same CAS 882423-09-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.21 g/mol
Formula C₈H₈F₃NO₂S
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry due to the presence of both the trifluoromethyl and sulfonamide groups, which are known to enhance metabolic stability and bioavailability. Also employed in agrochemical research for designing novel pesticides and herbicides, where the electron-withdrawing trifluoromethyl group improves compound efficacy and environmental persistence. Its structure allows for easy functionalization, making it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,580.00
inventory 5g
10-20 days ฿28,000.00

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n-Methyl-3-(trifluoromethyl)benzenesulfonamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry due to the presence of both the trifluoromethyl and sulfonamide groups, which are known to enhance metabolic stability and bioavailability. Also employed in agrochemical research for designing novel pesticides and herbicides, where the electron-withdrawing trifluoromethyl

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of sulfonamide-based drugs with potential antimicrobial and anti-inflammatory properties. It serves as a building block in medicinal chemistry due to the presence of both the trifluoromethyl and sulfonamide groups, which are known to enhance metabolic stability and bioavailability. Also employed in agrochemical research for designing novel pesticides and herbicides, where the electron-withdrawing trifluoromethyl group improves compound efficacy and environmental persistence. Its structure allows for easy functionalization, making it valuable in combinatorial chemistry and high-throughput screening for drug discovery.

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