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CAS 220497-90-5

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(R)-N-FMOC-3-Thienylalanine

Description:
(R)-N-FMOC-3-Thienylalanine is a synthetic amino acid derivative characterized by the presence of a thienyl group, which is a five-membered aromatic ring containing sulfur. The "FMOC" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, commonly used in peptide synthesis to prevent unwanted reactions during the coupling process. This compound is chiral, with the "(R)" designation indicating the specific spatial arrangement of its atoms, which can influence its biological activity and interactions. The thienyl moiety contributes to the compound's hydrophobic characteristics, potentially affecting its solubility and reactivity. As a building block in peptide synthesis, (R)-N-FMOC-3-Thienylalanine is valuable in the development of peptides with specific structural and functional properties, particularly in medicinal chemistry and drug design. Its unique structure allows for the exploration of novel therapeutic agents, especially in the context of targeting specific biological pathways or receptors.
Formula:C22H19NO4S
InChI:InChI=1/C22H19NO4S/c24-21(25)20(11-14-9-10-28-13-14)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-/m1/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@H](Cc1ccsc1)C(=O)O)O
Synonyms:
  • N-(9-Fluorenylmethoxycarbonyl)-3-thienyl-D-alanine
  • Fmoc-D-3-Thienylalanine
  • Fmoc-beta-(3-thienyl)-D-Ala-OH
  • (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-thiophen-3-ylpropanoate
  • N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-thiophen-3-yl-D-alanine
  • Fmoc-D-3-(3-Thienyl)alanine
  • Fmoc-3-(3-Thienyl)-D-alanine
  • (R)-N-FMOC-3-Thienylalanine, 98% ee
  • Fmoc-β-(3-thienyl)-D-alanine
  • FMOC-D-(3)THG-OH
  • See more synonyms
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