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Structure of 188348-00-7
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This chiral carbamate features a tert-butyl-protected hydroxyl group and a cyclohexyl-substituted ethyl scaffold, enabling straightforward deprotection under mild acidic conditions. The (R)-configuration provides stereochemical fidelity in asymmetric synthesis, while the bench-stable, moisture-tolerant nature simplifies handling in multi-step workflows.
tert-Butyl (R)-(1-cyclohexyl-2-hydroxyethyl)carbamate serves as a chiral auxiliary and protected amino alcohol synthon, enabling stereoselective transformations in asymmetric synthesis. The tert-butyl carbamate group provides robust protection for primary amines, while the hydroxyl functionality supports orthogonal derivatization. Its bench-stable nature and compatibility with standard coupling and reduction protocols make it a practical building block for complex molecule assembly.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335-H410
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Precautionary Statements : P261-P264-P270-P271-P273-P280-P302+P352-P304+P340-P330-P362+P364-P391-P405-P501
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Lot numbers can be found on the outside label of a product: