CymitQuimica logo

CAS 511272-45-0

:

(3S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-thiophen-2-ylpropanoic acid

Description:
The chemical substance known as (3S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-thiophen-2-ylpropanoic acid, with the CAS number 511272-45-0, is a synthetic compound that features a thiophene ring, an amino acid structure, and a protective fluorenylmethoxycarbonyl (Fmoc) group. This compound is characterized by its chiral center at the 3-position of the propanoic acid backbone, which contributes to its stereochemical properties. The presence of the thiophene moiety imparts unique electronic and structural characteristics, making it of interest in medicinal chemistry and drug design. The Fmoc group is commonly used in peptide synthesis as a protecting group for amino acids, allowing for selective reactions. The compound's solubility, stability, and reactivity can vary based on its functional groups and the surrounding environment, making it suitable for various applications in organic synthesis and biochemistry. Overall, this compound exemplifies the intersection of organic chemistry and pharmaceutical development, highlighting the importance of structural features in determining biological activity.
Formula:C22H19NO4S
InChI:InChI=1/C22H19NO4S/c24-21(25)12-19(20-10-5-11-28-20)23-22(26)27-13-18-16-8-3-1-6-14(16)15-7-2-4-9-17(15)18/h1-11,18-19H,12-13H2,(H,23,26)(H,24,25)/t19-/m0/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@@H](CC(=O)O)c1cccs1)O
Synonyms:
  • (3S)-3-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-(2-thienyl)propanoic acid
  • 2-thiophenepropanoic acid, beta-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (betaS)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.