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CAS 69901-85-5

:

(αR)-α-[[(Phenylmethoxy)carbonyl]amino]cyclohexaneacetic acid

Description:
(αR)-α-[[(Phenylmethoxy)carbonyl]amino]cyclohexaneacetic acid, with CAS number 69901-85-5, is a chiral amino acid derivative characterized by its cyclohexane structure and the presence of a phenylmethoxycarbonyl group. This compound typically exhibits properties associated with amino acids, such as the ability to form hydrogen bonds and participate in various chemical reactions due to its functional groups. The presence of the phenylmethoxycarbonyl moiety enhances its lipophilicity, potentially influencing its solubility and reactivity in organic solvents. As a chiral molecule, it can exist in two enantiomeric forms, which may exhibit different biological activities or pharmacological effects. The cyclohexane ring contributes to its three-dimensional conformation, which is crucial for interactions with biological targets. This compound may be of interest in pharmaceutical research, particularly in the development of drugs that target specific biological pathways or receptors. Its synthesis and characterization would involve standard organic chemistry techniques, including protection-deprotection strategies and chiral resolution methods.
Formula:C16H21NO4
InChI:InChI=1S/C16H21NO4/c18-15(19)14(13-9-5-2-6-10-13)17-16(20)21-11-12-7-3-1-4-8-12/h1,3-4,7-8,13-14H,2,5-6,9-11H2,(H,17,20)(H,18,19)/t14-/m1/s1
InChI key:InChIKey=CUSYTUPJAYLNFQ-CQSZACIVSA-N
SMILES:[C@H](NC(OCC1=CC=CC=C1)=O)(C(O)=O)C2CCCCC2
Synonyms:
  • (R)-2-(((Benzyloxy)carbonyl)amino)-2-cyclohexylacetic acid
  • (R)-2-(((Benzyloxy)carbonyl)amino)-2-cyclohexylaceticacid
  • (αR)-α-[[(Phenylmethoxy)carbonyl]amino]cyclohexaneacetic acid
  • CBZ-D-Chg-OH
  • Cbz-D-Cyclohexyl glycine
  • Cyclohexaneacetic acid, α-[[(phenylmethoxy)carbonyl]amino]-, (R)-
  • Cyclohexaneacetic acid, α-[[(phenylmethoxy)carbonyl]amino]-, (αR)-
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