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Structure of 77119-85-8
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(R)-tert-Butyl (1-oxo-3-phenylpropan-2-yl)carbamate is a chiral building block featuring a stereodefined quaternary center, enabling precise asymmetric synthesis. The carbamate group provides stable protection for amine functionalities, while the phenyl-substituted ketone moiety offers a handle for further functionalization. This scaffold integrates readily into complex molecular architectures under standard conditions.
(R)-tert-Butyl (1-oxo-3-phenylpropan-2-yl)carbamate serves as a chiral building block for synthesizing biologically active molecules, enabling efficient access to enantiomerically pure α-aryl-β-keto amine motifs. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate straightforward transformations in medicinal chemistry workflows. The carbamate protecting group allows for selective deprotection and further derivatization, supporting scalable synthesis of complex heterocyclic scaffolds and API intermediates.
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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: