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Structure of 155975-19-2
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tert-Butyl ((1R,2R)-2-hydroxycyclohexyl)carbamate is a chiral auxiliary featuring a rigid cyclohexane scaffold with a stereodefined hydroxyl group and a bench-stable carbamate protecting group. This configuration enables selective functionalization in asymmetric synthesis, particularly in the installation of stereocenters via dihydroxylation or oxidation protocols. The protected alcohol remains inert under many reaction conditions while allowing controlled deprotection post-functionalization.
tert-Butyl ((1R,2R)-2-hydroxycyclohexyl)carbamate serves as a stereochemically defined chiral building block for cyclohexane-based scaffolds. The protected amine and secondary alcohol functionalities enable orthogonal derivatization in synthetic sequences. Its bench-stable nature and compatibility with standard coupling and reduction protocols facilitate efficient access to complex cyclic architectures. Functions effectively in asymmetric synthesis and medicinal chemistry campaigns requiring rigid, stereoregular frameworks.
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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: