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Structure of 197020-60-3
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(S)-tert-Butyl 2-methylaziridine-1-carboxylate features a chiral aziridine core with a methyl group at the 2-position, enabling stereoselective transformations. The tert-butyl carbamate protecting group ensures stability and ease of handling under standard conditions. This bench-stable reagent integrates readily into asymmetric synthesis workflows, delivering controlled ring-opening reactions for complex nitrogen heterocycles.
(S)-tert-Butyl 2-methylaziridine-1-carboxylate serves as a chiral building block for the synthesis of bioactive nitrogen-containing heterocycles. Its strained aziridine ring enables regioselective ring-opening reactions with nucleophiles, facilitating the installation of diverse functional groups under mild conditions. The tert-butyl carbamate group provides excellent stability and ease of removal during late-stage deprotection, enhancing its utility in medicinal chemistry workflows.
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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-P362+P364-P370+P378-P501
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Lot numbers can be found on the outside label of a product: