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CAS 103322-56-1

:

(S)-(-)-2-(tert-butoxycarbonylamino)-3-cyclohexyl

Description:
(S)-(-)-2-(tert-butoxycarbonylamino)-3-cyclohexyl is an organic compound characterized by its specific stereochemistry and functional groups. The presence of the tert-butoxycarbonyl (Boc) group indicates that it is a protected amino acid derivative, commonly used in peptide synthesis to temporarily shield the amino group from reactions. The cyclohexyl group contributes to the compound's hydrophobic characteristics, influencing its solubility and interaction with biological systems. The compound's chirality, denoted by the (S)- configuration, suggests that it has a specific three-dimensional arrangement that can affect its biological activity and reactivity. This compound is typically utilized in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals. Its stability, reactivity, and solubility can vary based on environmental conditions such as pH and temperature, making it essential to consider these factors during handling and application. Overall, this compound exemplifies the complexity and utility of chiral organic molecules in chemical research and development.
Formula:C14H27NO3
InChI:InChI=1/C14H27NO3/c1-14(2,3)18-13(17)15-12(10-16)9-11-7-5-4-6-8-11/h11-12,16H,4-10H2,1-3H3,(H,15,17)/t12-/m0/s1
SMILES:CC(C)(C)OC(=N[C@@H](CC1CCCCC1)CO)O
Synonyms:
  • (S)-(?-2-(tert-Butoxycarbonylamino)-3-cyclohexyl-1-propanol
  • Boc-.beta.-cyclohexyl-L-alaninol
  • tert-butyl [(1S)-2-cyclohexyl-1-(hydroxymethyl)ethyl]carbamate
  • BOC-3-CYCLOHEXYL-L-ALANINOL
  • (s)-(-)-2-N-Boc-3-cyclohexyl-1-propanol
  • ert-butylN-[(2S)-1-cyclohexyl-3-hydroxypropan-2-yl]carbamate
  • N-T-BUTOXYCARBONYL-L-CYCLOHEXYLALANINOL
  • (S)-(-)-2-(t-Butoxycarbonylamino)-3-cyclohexyl-1-propanol, 90%
  • (S)-(-)-2-(Boc-amino)-3-cyclohexyl-1-propanol
  • (S)-(-)-2-(tert-butoxycarbonylamino)-3-cyclohexyl
  • See more synonyms
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