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Structure of 52206-05-0
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1-Acetyl-2,3-dihydro-1H-indole-5-sulfonyl chloride features a reactive sulfonyl chloride group flanked by an acetylated indoline core, enabling direct incorporation into amide-linked architectures. This bench-stable derivative delivers efficient conjugation in synthetic workflows requiring site-specific functionalization.
1-Acetyl-2,3-dihydro-1H-indole-5-sulfonyl chloride serves as a versatile sulfonylating agent for the introduction of sulfonamide groups under mild conditions. Its acetyl-protected indoline scaffold enables direct functionalization at nitrogen and facilitates downstream derivatization in medicinal chemistry campaigns. The reagent exhibits good bench stability and compatibility with common functional groups, enabling efficient synthesis of heterocyclic scaffolds relevant to API 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#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: