3-Bromo-5-(trifluoromethyl)benzenesulfonyl chloride

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Reagent Code: #144853
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CAS Number 351003-46-8

science Other reagents with same CAS 351003-46-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.51 g/mol
Formula C₇H₃BrClF₃O₂S
badge Registry Numbers
MDL Number MFCD03094393
thermostat Physical Properties
Boiling Point 217-218°C - (Lit.)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in drug development, particularly in the creation of sulfonamide-based compounds with biological activity. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules due to the electron-withdrawing nature of the trifluoromethyl and sulfonyl groups. Also utilized in materials science for designing specialty polymers with enhanced thermal and oxidative stability. The bromine moiety enables further cross-coupling reactions, making it valuable in modular synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,620.00
inventory 10g
10-20 days ฿2,980.00
inventory 25g
10-20 days ฿4,790.00
inventory 100g
10-20 days ฿19,070.00
inventory 500g
10-20 days ฿82,840.00

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3-Bromo-5-(trifluoromethyl)benzenesulfonyl chloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in drug development, particularly in the creation of sulfonamide-based compounds with biological activity. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules due to the electron-withdrawing nature of the trifluoromethyl and sulfonyl groups. Also utilized in materials science for designing specialty polymers with enhanced ther

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in drug development, particularly in the creation of sulfonamide-based compounds with biological activity. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules due to the electron-withdrawing nature of the trifluoromethyl and sulfonyl groups. Also utilized in materials science for designing specialty polymers with enhanced thermal and oxidative stability. The bromine moiety enables further cross-coupling reactions, making it valuable in modular synthetic routes.

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