2-Nitro-4-((trifluoromethyl)sulfonyl)phenol

97%

Reagent Code: #219324
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CAS Number 15183-75-2

science Other reagents with same CAS 15183-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.17 g/mol
Formula C₇H₄F₃NO₅S
badge Registry Numbers
MDL Number MFCD00986405
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its nitro and trifluoromethylsulfonyl functional groups make it valuable in building complex organic molecules through reduction, coupling, and nucleophilic substitution reactions. Commonly employed in research settings for designing sulfone-based bioactive compounds. Also serves as a precursor in the preparation of dyes and functional materials where electron-withdrawing groups enhance stability and reactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,990.00
inventory 250mg
10-20 days ฿5,090.00
inventory 1g
10-20 days ฿13,750.00
2-Nitro-4-((trifluoromethyl)sulfonyl)phenol
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its nitro and trifluoromethylsulfonyl functional groups make it valuable in building complex organic molecules through reduction, coupling, and nucleophilic substitution reactions. Commonly employed in research settings for designing sulfone-based bioactive compounds. Also serves as a precursor in the preparation of dyes and functional materials where electron-withd

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its nitro and trifluoromethylsulfonyl functional groups make it valuable in building complex organic molecules through reduction, coupling, and nucleophilic substitution reactions. Commonly employed in research settings for designing sulfone-based bioactive compounds. Also serves as a precursor in the preparation of dyes and functional materials where electron-withdrawing groups enhance stability and reactivity.

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