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CAS 270262-98-1

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

Description:
Fmoc-(S)-3-amino-4-(2-thienyl)-butyric acid is a chemical compound commonly used in peptide synthesis and drug development. It features a phenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized to protect amino groups during the synthesis of peptides. The compound contains a chiral center, indicated by the (S) configuration, which is crucial for its biological activity and interaction with receptors. The presence of a thienyl group contributes to its unique electronic and steric properties, potentially influencing its solubility and reactivity. This compound is typically characterized by its solid-state form, stability under standard laboratory conditions, and its ability to participate in various coupling reactions. Its applications extend to the synthesis of biologically active peptides, where the thienyl moiety may enhance pharmacological properties. As with many amino acids and derivatives, it is essential to handle this compound with care, following appropriate safety protocols due to potential biological activity and reactivity.
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-/m1/s1
Synonyms:
  • (3S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-thiophen-2-ylbutanoic acid
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