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Structure of 10438-96-7
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N-Methylsulfamoyl chloride features a reactive sulfonyl chloride group paired with a methyl-substituted nitrogen, enabling efficient incorporation into pharmaceutical intermediates. This bench-stable reagent facilitates rapid amide bond formation and sulfonamide synthesis under mild conditions, offering high functional group tolerance and clean reaction profiles.
N-Methylsulfamoyl chloride serves as a versatile acylating agent for the direct introduction of the sulfamoyl group into organic substrates. It facilitates efficient amide bond formation with amines under mild conditions, offering high functional group tolerance and ease of handling in synthetic workflows. Its bench stability and clean reaction profile make it a practical choice for building sulfonamide-containing scaffolds in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1760
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H312-H314-H332
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: