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CAS 511272-52-9

:

(3R)-3-(2-chlorophenyl)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid

Description:
The chemical substance known as (3R)-3-(2-chlorophenyl)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid, with the CAS number 511272-52-9, is a synthetic compound that features a chiral center, indicating it exists in two enantiomeric forms. This compound is characterized by the presence of a propanoic acid backbone, which is substituted with a 2-chlorophenyl group and a fluorenylmethoxycarbonyl (Fmoc) protecting group on the amino functionality. The Fmoc group is commonly used in peptide synthesis to protect amino groups during the formation of peptide bonds. The presence of the chlorophenyl moiety may impart specific electronic and steric properties, influencing its reactivity and interactions in biological systems. This compound is likely to be of interest in medicinal chemistry and peptide synthesis due to its structural features, which may contribute to its biological activity or utility in drug development. As with many synthetic compounds, its solubility, stability, and reactivity would depend on the specific conditions under which it is handled.
Formula:C24H20ClNO4
InChI:InChI=1/C24H20ClNO4/c25-21-12-6-5-11-19(21)22(13-23(27)28)26-24(29)30-14-20-17-9-3-1-7-15(17)16-8-2-4-10-18(16)20/h1-12,20,22H,13-14H2,(H,26,29)(H,27,28)/t22-/m1/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@H](CC(=O)O)c1ccccc1Cl)O
Synonyms:
  • benzenepropanoic acid, 2-chloro-beta-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (betaR)-
  • Fmoc-(R)-3-Amino-3-(2-chlorophenyl)-propionic acid
  • Fmoc-(R)-3-Amino-3-(2-Chloro-Phenyl)-Propionic Acid
  • (3R)-3-(2-Chlorophenyl)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoic acid
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