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CAS 269726-90-1

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Fmoc-(R)-3-amino-4-(2-thienyl)-butyric acid

Description:
Fmoc-(R)-3-amino-4-(2-thienyl)-butyric acid is a chemical compound characterized by its structure, which includes a thienyl group and an Fmoc (9-fluorenylmethoxycarbonyl) protecting group. This compound is an amino acid derivative, specifically an enantiomer of a substituted butyric acid, which contributes to its potential applications in peptide synthesis and drug development. The presence of the thienyl moiety may impart unique electronic and steric properties, making it useful in various biochemical applications. The Fmoc group serves as a protective group for the amino functionality, allowing for selective reactions during peptide synthesis. This compound is typically used in research settings, particularly in the fields of medicinal chemistry and organic synthesis, where it can facilitate the development of novel therapeutic agents. Its solubility and stability characteristics are influenced by the functional groups present, and it is essential to handle it under appropriate laboratory conditions to maintain its integrity.
Formula:C23H21NO4S
InChI:InChI=1/C23H21NO4S/c25-22(26)13-15(12-16-6-5-11-29-16)24-23(27)28-14-21-19-9-3-1-7-17(19)18-8-2-4-10-20(18)21/h1-11,15,21H,12-14H2,(H,24,27)(H,25,26)/t15-/m0/s1
Synonyms:
  • (3R)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-thiophen-2-ylbutanoic acid
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