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Structure of 1803033-61-5
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tert-Butyl N-[(1S)-3-oxocyclohexyl]carbamate features a chiral cyclohexanone-derived scaffold with a bench-stable carbamate protecting group. This configuration enables selective functionalization at the carbonyl site while maintaining stereochemical integrity during downstream transformations. The tert-butyl moiety facilitates easy deprotection under mild acidic conditions, streamlining access to enantiopure amine intermediates for complex molecule synthesis.
tert-Butyl N-[(1S)-3-oxocyclohexyl]carbamate serves as a chiral, bench-stable building block for asymmetric synthesis, enabling direct functionalization at the C3 carbonyl position while the tert-butoxycarbonyl (Boc) group provides orthogonal protection. Its rigid cyclohexanone framework facilitates stereoselective transformations and supports downstream applications in heterocycle construction and medicinal chemistry scaffolds.
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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: