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Structure of 63177-41-3
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1-(Azetidin-1-yl)-2-chloroethan-1-one features a reactive acyl chloride moiety paired with a strained azetidine ring, enabling efficient conjugation in synthetic transformations. This electrophilic scaffold integrates readily into peptide and heterocyclic architectures under mild conditions. The compound exhibits enhanced stability compared to analogous reagents, facilitating handling in standard bench protocols.
1-(Azetidin-1-yl)-2-chloroethan-1-one serves as a versatile acylating agent in synthetic organic chemistry, enabling efficient introduction of the azetidinyl carbonyl moiety into target molecules. Its reactivity facilitates nucleophilic acyl substitution under mild conditions, with good bench stability and compatibility across diverse functional groups. This compound functions as a key building block for constructing nitrogen-containing heterocycles and bioactive scaffolds, particularly in medicinal chemistry campaigns requiring constrained amide linkages.
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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#: 3265
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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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: