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tert-Butyl N-[(1S)-3-oxocyclohexyl]carbamate

  • CAS No. 1803033-61-5

  • Cat. No. CS-0048035
  • Purity≥95%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

tert-Butyl N-[(1S)-3-oxocyclohexyl]carbamate|CS-0048035

Structure of 1803033-61-5

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General Information

  • CAS No. 1803033-61-5
  • Cat. No. CS-0048035
  • Purity ≥95%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₉NO₃
  • Molecular Weight 213.27
  • Synonym(s) tert-butyl (S)-(3-oxocyclohexyl)carbamate
  • SMILES CC(C)(C)OC(=O)N[C@H]1CCCC(=O)C1

Description

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.

Application

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.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
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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Computational Chemistry Data

  • TPSA   55.4
  • LogP   2.0228
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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