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Structure of 154632-86-7
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(R)-1-Benzyl 2-methyl aziridine-1,2-dicarboxylate is a chiral aziridine derivative featuring a strained three-membered ring with defined stereochemistry. This bench-stable compound integrates a benzyl ester and methyl substituent, enabling selective ring-opening reactions in asymmetric synthesis. The electron-deficient aziridine moiety facilitates nucleophilic attack under mild conditions, making it valuable for constructing complex nitrogen-containing scaffolds in medicinal chemistry and natural product synthesis.
(R)-1-Benzyl 2-methyl aziridine-1,2-dicarboxylate serves as a chiral building block for the synthesis of biologically active compounds, enabling stereoselective ring-opening reactions. Its stable aziridine core tolerates diverse nucleophiles and functions effectively in asymmetric synthesis workflows. The benzyl and methyl ester groups provide orthogonal handles for selective transformations, facilitating purification and downstream functionalization. This compound is particularly useful in constructing nitrogen-containing heterocycles and peptide-like scaffolds under standard bench conditions.
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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: