CAS 507472-09-5
:(3S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-thiophen-3-ylpropanoic acid
Description:
The chemical substance known as (3S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-thiophen-3-ylpropanoic acid, with the CAS number 507472-09-5, is an amino acid derivative characterized by the presence of a thiophene ring and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound features a chiral center at the 3-position, which contributes 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 thiophene moiety adds to the compound's structural complexity and may influence its solubility and reactivity. This substance is of interest in medicinal chemistry and peptide synthesis, where its unique structure can be leveraged for the development of novel therapeutic agents. Its properties, such as solubility, melting point, and reactivity, would depend on the specific conditions and solvents used in experiments or applications.
Formula:C22H19NO4S
InChI:InChI=1/C22H19NO4S/c24-21(25)11-20(14-9-10-28-13-14)23-22(26)27-12-19-17-7-3-1-5-15(17)16-6-2-4-8-18(16)19/h1-10,13,19-20H,11-12H2,(H,23,26)(H,24,25)/t20-/m0/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@@H](CC(=O)O)c1ccsc1)O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
Fmoc-(S)-3-Amino-3-(3-thienyl)-propionic acid
CAS:Formula:C22H19NO4SPurity:95%Color and Shape:SolidMolecular weight:393.4556Fmoc-(S)-3-Amino-3-(3-thienyl)-propionic acid
CAS:Fmoc-(S)-3-Amino-3-(3-thienyl)-propionic acidPurity:95%Molecular weight:393.46g/mol(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(thiophen-3-yl)propanoic acid
CAS:Formula:C22H19NO4SPurity:95%Molecular weight:393.46


