3-Bromomethylbenzenesulfonyl chloride

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Reagent Code: #154591
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CAS Number 148583-69-1

science Other reagents with same CAS 148583-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.54 g/mol
Formula C₇H₆BrClO₂S
badge Registry Numbers
MDL Number MFCD09743701
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive bromomethyl and sulfonyl chloride functional groups allow for selective derivatization, making it valuable in constructing sulfonamide-based compounds. Commonly employed in the preparation of protease inhibitors and other biologically active molecules. Also utilized in organic synthesis for introducing benzenesulfonyl moieties in peptide chemistry and in the development of labeled compounds for research. Its dual reactivity enables sequential functionalization, useful in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,830.00
inventory 250mg
10-20 days ฿21,510.00
inventory 1g
10-20 days ฿65,960.00

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3-Bromomethylbenzenesulfonyl chloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive bromomethyl and sulfonyl chloride functional groups allow for selective derivatization, making it valuable in constructing sulfonamide-based compounds. Commonly employed in the preparation of protease inhibitors and other biologically active molecules. Also utilized in organic synthesis for introducing benzenesulfonyl moieties in peptide chemistry and in the development of labeled compounds for resear

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive bromomethyl and sulfonyl chloride functional groups allow for selective derivatization, making it valuable in constructing sulfonamide-based compounds. Commonly employed in the preparation of protease inhibitors and other biologically active molecules. Also utilized in organic synthesis for introducing benzenesulfonyl moieties in peptide chemistry and in the development of labeled compounds for research. Its dual reactivity enables sequential functionalization, useful in multi-step synthetic routes.

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