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Structure of 137102-65-9
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(R)-tert-Butyl (2-amino-1-phenylethyl)carbamate is a chiral building block featuring a stereodefined amino alcohol scaffold. This bench-stable, moisture-tolerant reagent integrates readily into asymmetric synthesis workflows. The protected amine and phenyl-substituted carbon center enable direct functionalization in peptide mimicry and catalytic transformations.
(R)-tert-Butyl (2-amino-1-phenylethyl)carbamate serves as a key chiral building block in asymmetric synthesis, enabling the stereoselective construction of phenylethylamine derivatives. Its robust tert-butyl carbamate protecting group offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The molecule functions effectively in peptide coupling, reductive amination, and transition-metal-catalyzed transformations, providing access to biologically relevant scaffolds with high enantiomeric purity.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: