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rel-tert-Butyl ((1R,4R)-4-aminocyclohexyl)(methyl)carbamate

  • CAS No. 566172-79-0

  • Cat. No. CS-0504766
  • Purity≥96%
  • MDL No.MFCD17014916

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

rel-tert-Butyl ((1R,4R)-4-aminocyclohexyl)(methyl)carbamate|CS-0504766

Structure of 566172-79-0

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General Information

  • CAS No. 566172-79-0
  • Cat. No. CS-0504766
  • Purity ≥96%
  • MDL No. MFCD17014916
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₂₄N₂O₂
  • Molecular Weight 228.33
  • Synonym(s) trans-N-Boc-N-methyl-1,4-cyclohexanediamine
  • SMILES CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](N)CC1

Description

Tert-butyl ((1r,4r)-4-aminocyclohexyl)(methyl)carbamate is a bench-stable, moisture-tolerant amine-containing building block featuring a rigid cyclohexyl scaffold. The (1r,4r) stereochemistry ensures defined spatial orientation, while the tert-butyl carbamate group enables protection and controlled deprotection under standard conditions. This compound integrates readily into peptide-like architectures and serves as a key intermediate in the synthesis of bioactive molecules requiring a constrained, functionalized amine handle.

Application

Tert-butyl ((1r,4r)-4-aminocyclohexyl)(methyl)carbamate serves as a versatile, bench-stable building block for the synthesis of bioactive cyclohexane-containing compounds. The (1r,4r)-configured amine enables stereocontrolled functionalization, while the tert-butyl carbamate group provides orthogonal protection compatible with standard deprotection protocols. Its methylcarbamate moiety enhances solubility and facilitates purification, making it ideal for iterative peptide-like coupling strategies and medicinal chemistry campaigns requiring precise stereochemical control.

Safety Information

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GHS Pictogram :
GHS No : GHS05,GHS07,GHS09
Signal Word : Danger
UN#: 3077
Class : 9
Packing Group : Ⅲ
Hazard Statements : H302-H318-H410
Precautionary Statements : P264-P270-P273-P280-P330-P391-P501

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Computational Chemistry Data

  • TPSA   55.56
  • LogP   2.1232
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   1

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