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CAS 478183-63-0

:

(αR)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclobutanepropanoic acid

Description:
(αR)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclobutanepropanoic acid is a synthetic amino acid derivative characterized by its unique structural features. This compound contains a cyclobutane ring, which contributes to its rigidity and influences its conformational properties. The presence of the fluorenylmethoxycarbonyl (Fmoc) group serves as a protective moiety for the amino group, commonly utilized in peptide synthesis to facilitate the formation of peptide bonds while preventing unwanted reactions. The compound's chirality, indicated by the (αR) designation, suggests that it exhibits specific stereochemical properties, which can significantly affect its biological activity and interaction with enzymes or receptors. Additionally, the carboxylic acid functional group imparts acidic characteristics, allowing for potential solubility in polar solvents and participation in acid-base reactions. Overall, this compound is of interest in medicinal chemistry and peptide synthesis due to its structural complexity and potential applications in drug development.
Formula:C22H23NO4
InChI:InChI=1S/C22H23NO4/c24-21(25)20(12-14-6-5-7-14)23-22(26)27-13-19-17-10-3-1-8-15(17)16-9-2-4-11-18(16)19/h1-4,8-11,14,19-20H,5-7,12-13H2,(H,23,26)(H,24,25)/t20-/m1/s1
InChI key:InChIKey=FOJRBUNCWCPLNH-HXUWFJFHSA-N
SMILES:C(OC(N[C@H](CC1CCC1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • (αR)-α-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]cyclobutanepropanoic acid
  • Cyclobutanepropanoic acid, α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αR)-
  • Fmoc-(R)-3-Cyclobutylalanine
  • Fmoc-Beta-Cyclobutyl-D-Ala-Oh
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