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Structure of 160233-42-1
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Methyl (2R)-1-(triphenylmethyl)aziridine-2-carboxylate is a chiral aziridine derivative featuring a sterically encumbered triphenylmethyl group that stabilizes the strained three-membered ring. This bench-stable, moisture-tolerant reagent enables direct functionalization of aziridines in asymmetric synthesis. The ester functionality facilitates downstream derivatization, while the (2R) stereochemistry ensures high diastereoselectivity in nucleophilic ring-opening reactions.
Methyl (2R)-1-(triphenylmethyl)aziridine-2-carboxylate serves as a stable, bench-ready chiral building block for asymmetric synthesis. The triphenylmethyl (Trt) group provides robust protection of the aziridine nitrogen, enabling selective ring-opening reactions with nucleophiles under mild conditions. Its inherent chirality and functional group tolerance facilitate the construction of complex heterocyclic scaffolds and amino acid derivatives relevant to medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: