2-Chloro-4-(trifluoromethyl)benzenesulfonamide

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Reagent Code: #77134
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CAS Number 146533-47-3

science Other reagents with same CAS 146533-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.63 g/mol
Formula C₇H₅ClF₃NO₂S
badge Registry Numbers
MDL Number MFCD00179384
thermostat Physical Properties
Melting Point 168-171° C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in the synthesis of agrochemicals, particularly as an intermediate in the production of herbicides. It plays a key role in creating active ingredients that target broadleaf weeds and grasses in crops, enhancing agricultural productivity. Additionally, it is utilized in pharmaceutical research for developing sulfonamide-based drugs, which are known for their antimicrobial properties. Its trifluoromethyl group contributes to the stability and efficacy of the final products, making it valuable in both agricultural and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,224.00

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2-Chloro-4-(trifluoromethyl)benzenesulfonamide
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This compound is primarily used in the synthesis of agrochemicals, particularly as an intermediate in the production of herbicides. It plays a key role in creating active ingredients that target broadleaf weeds and grasses in crops, enhancing agricultural productivity. Additionally, it is utilized in pharmaceutical research for developing sulfonamide-based drugs, which are known for their antimicrobial properties. Its trifluoromethyl group contributes to the stability and efficacy of the final products,

This compound is primarily used in the synthesis of agrochemicals, particularly as an intermediate in the production of herbicides. It plays a key role in creating active ingredients that target broadleaf weeds and grasses in crops, enhancing agricultural productivity. Additionally, it is utilized in pharmaceutical research for developing sulfonamide-based drugs, which are known for their antimicrobial properties. Its trifluoromethyl group contributes to the stability and efficacy of the final products, making it valuable in both agricultural and medicinal chemistry.

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