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Structure of 50487-72-4
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N,N-Diallyl-4-methylbenzenesulfonamide features a sulfonamide core with two diallyl substituents, enabling efficient incorporation into polymer networks via thiol-ene click chemistry. The para-methyl group enhances electron density at the aromatic ring, improving reactivity in conjugate addition processes. This bench-stable, moisture-tolerant compound serves as a robust building block for functionalized materials and bioconjugation scaffolds.
N,N-Diallyl-4-methylbenzenesulfonamide serves as a versatile sulfonamide building block in synthetic organic chemistry, enabling efficient access to functionalized heterocycles and conjugated systems. The diallyl moiety facilitates [3+2] cycloaddition and radical polymerization reactions, while the sulfonamide group provides excellent stability and orthogonal reactivity. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry and materials synthesis workflows.
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: