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Structure of 42137-88-2
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N,N-Bis(2-chloroethyl)-4-methylbenzenesulfonamide features a sulfonamide core with two 2-chloroethyl substituents, enabling dual alkylating potential. The para-methyl group enhances electron density at the aromatic ring, improving stability under standard conditions. This compound functions as a bifunctional electrophile in targeted covalent labeling and crosslinking applications.
N,N-Bis(2-chloroethyl)-4-methylbenzenesulfonamide serves as a versatile bifunctional electrophile, enabling efficient sulfonamide-directed conjugate additions and tandem cyclizations. Its dual 2-chloroethyl groups facilitate rapid, high-yield intramolecular cyclization under mild conditions, forming stable heterocyclic scaffolds. Bench-stable and compatible with diverse functional groups, it functions as a key building block in the synthesis of complex sulfonamide-containing frameworks relevant to medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: