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Structure of 181212-90-8
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1-tert-Butyl 2-methyl aziridine-1,2-dicarboxylate is a bench-stable, sterically hindered aziridine derivative featuring two ester-protected nitrogen functionalities. This configuration enables selective ring-opening reactions under mild conditions, facilitating the synthesis of chiral amino acid derivatives and complex heterocycles in medicinal chemistry workflows.
1-tert-Butyl 2-methyl aziridine-1,2-dicarboxylate serves as a versatile chiral building block in asymmetric synthesis, enabling stereoselective ring-opening reactions with nucleophiles. Its strained aziridine core facilitates regioselective functionalization under mild conditions, while the dicarboxylate protecting groups offer stability and ease of purification. This compound functions effectively in the construction of complex heterocycles and amino acid derivatives relevant to medicinal chemistry.
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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: