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Structure of 82353-56-8
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tert-Butyl (R)-(1-oxopropan-2-yl)carbamate is a chiral protecting group reagent featuring a stereodefined (R)-configuration at the prochiral carbon. This bench-stable carbamate delivers selective N-protection in asymmetric synthesis, enabling efficient incorporation into complex peptide architectures and chiral building blocks without racemization.
tert-Butyl (R)-(1-oxopropan-2-yl)carbamate serves as a stereochemically defined chiral auxiliary and protected amino acid precursor, enabling efficient enantioselective synthesis of β-amino carbonyl compounds. Its tert-butyl carbamate group offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The molecule functions reliably in peptide coupling, asymmetric alkylation, and nucleophilic addition reactions, providing high diastereoselectivity in standard synthetic 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: