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CAS 312965-07-4

:

(1S,2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid

Description:
The chemical substance known as (1S,2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid, with the CAS number 312965-07-4, is a derivative of cyclohexanecarboxylic acid featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is characterized by its chiral centers, which contribute to its stereochemistry and potential biological activity. The Fmoc group is commonly used in peptide synthesis as a protective group for amino acids, allowing for selective reactions without interfering with the amine functionality. The presence of the cyclohexane ring adds rigidity to the molecular structure, influencing its conformational properties and interactions. This compound is typically utilized in organic synthesis and peptide chemistry, particularly in the development of pharmaceuticals and biologically active molecules. Its solubility and stability in various solvents can vary, making it important to consider these factors during experimental applications. Overall, this compound exemplifies the complexity and utility of modified amino acids in chemical research and drug development.
Formula:C22H23NO4
InChI:InChI=1S/C22H23NO4/c24-21(25)18-11-5-6-12-20(18)23-22(26)27-13-19-16-9-3-1-7-14(16)15-8-2-4-10-17(15)19/h1-4,7-10,18-20H,5-6,11-13H2,(H,23,26)(H,24,25)/t18-,20-/m0/s1
InChI key:InChIKey=NZMNDTGOODAUNI-ICSRJNTNSA-N
SMILES:C(OC(N[C@@H]1[C@@H](C(O)=O)CCCC1)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (1S,2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclohexanecarboxylic acid
  • (1S,2S)-Fmoc-2-Aminocyclohexane Carboxylic Acid
  • (1S,2S)-Fmoc-Achc
  • Cyclohexanecarboxylic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (1S,2S)-
  • Fmoc-(1S,2S)-2-Aminocyclohexane Carboxylic Acid
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