3-Bromo-2-methylbenzene-1-sulfonyl chloride

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Reagent Code: #153647
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CAS Number 886501-61-7

science Other reagents with same CAS 886501-61-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.54 g/mol
Formula C₇H₆BrClO₂S
badge Registry Numbers
MDL Number MFCD07782194
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. Commonly employed in the development of herbicides and fungicides due to the enhanced bioactivity imparted by the sulfonyl moiety. Also utilized in medicinal chemistry for the preparation of kinase inhibitors and other biologically active molecules where the bromo and sulfonyl functionalities allow for further structural modifications through cross-coupling reactions or nucleophilic substitutions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,230.00
inventory 250mg
10-20 days ฿5,470.00

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3-Bromo-2-methylbenzene-1-sulfonyl chloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. Commonly employed in the development of herbicides and fungicides due to the enhanced bioactivity imparted by the sulfonyl moiety. Also utilized in medicinal chemistry for the preparation of kinase inhibitors and other biologically active molecules where the bromo an

Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. Commonly employed in the development of herbicides and fungicides due to the enhanced bioactivity imparted by the sulfonyl moiety. Also utilized in medicinal chemistry for the preparation of kinase inhibitors and other biologically active molecules where the bromo and sulfonyl functionalities allow for further structural modifications through cross-coupling reactions or nucleophilic substitutions.

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