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Structure of 97308-23-1
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tert-Butyl aziridine-1-carboxylate delivers a strained, reactive aziridine ring stabilized by a tert-butyl ester group. This bench-stable derivative enables direct incorporation of the aziridine moiety into synthetic sequences, facilitating nucleophilic ring-opening reactions under mild conditions.
tert-Butyl aziridine-1-carboxylate serves as a stable, bench-ready building block for the synthesis of nitrogen-containing heterocycles and chiral intermediates. Its aziridine ring enables regioselective ring-opening reactions with nucleophiles under mild conditions, while the tert-butyl carbamate group offers excellent stability and facile removal via acidolysis. Functions effectively in asymmetric synthesis and peptide-like scaffold construction due to its predictable reactivity and compatibility with diverse functional groups.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅱ
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Hazard Statements : H225-H315-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P264-P280-P302+P352-P362+P364-P370+P378-P501
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Lot numbers can be found on the outside label of a product: