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Structure of 39169-92-1
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4-(N-methylacetamido)benzenesulfonyl chloride features a sulfonyl chloride group flanked by an electron-rich aromatic ring and a sterically hindered N-methylacetamido substituent. This combination enables selective acylation in synthetic routes, particularly in the construction of sulfonamide-based bioactive compounds under standard conditions.
4-(N-methylacetamido)benzenesulfonyl chloride serves as a versatile sulfonylating agent for the efficient introduction of a substituted sulfonamide moiety into aromatic and heteroaromatic frameworks. Its amide-protected N-methyl group enhances bench stability and reduces hydrolytic sensitivity compared to parent analogs, while maintaining high reactivity toward nucleophiles such as amines and alcohols. The molecule facilitates straightforward access to functionalized sulfonamides relevant in medicinal chemistry and agrochemical synthesis, with purification typically achieved via crystallization or column chromatography.
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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#: 3261
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Class : 8
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Packing Group : Ⅱ
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Hazard Statements : H314-H318
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Precautionary Statements : P264-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: