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CAS 159611-02-6

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Fmoc-L-2-Furylalanine

Description:
Fmoc-L-2-Furylalanine is a derivative of the amino acid phenylalanine, characterized by the presence of a 2-furyl group attached to the alpha carbon of the amino acid. 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 typically utilized in the field of organic chemistry and peptide synthesis, particularly in the development of bioactive peptides and pharmaceuticals. Its structure allows for specific interactions due to the aromatic nature of the furyl group, which can influence the compound's solubility, stability, and reactivity. Fmoc-L-2-Furylalanine is generally soluble in organic solvents and exhibits properties typical of amino acids, such as the ability to form peptide bonds. The compound's unique features make it valuable in research and development, particularly in the synthesis of compounds with potential therapeutic applications.
Formula:C22H18NO5
InChI:InChI=1/C22H19NO5/c24-21(25)20(12-14-6-5-11-27-14)23-22(26)28-13-19-17-9-3-1-7-15(17)16-8-2-4-10-18(16)19/h1-11,19-20H,12-13H2,(H,23,26)(H,24,25)/p-1/t20-/m0/s1
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=N[C@@H](Cc1ccco1)C(=O)[O-])O
Synonyms:
  • (S)-2-(fmoc-amino)-3-(2-furyl)propionic acid
  • (S)-N-Fmoc-(2-Furyl)Alanine
  • (S)-N-Fmoc-Furylalanine
  • Rarechem Bk Pt 0223
  • N-Alpha-(9-Fluorenylmethoxycarbonyl)-2-Furylalanine-L-Phenylalanine
  • N-(9-Fluorenylmethoxycarbonyl)-2-Furyl-L-Alanine
  • Fmoc-3-Ala(2-Furyl)-Oh
  • Fmoc-3-(2-Furyl)-L-Alanine
  • Fmoc-L-3-(2-Furyl)-Alanine
  • N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-furan-2-yl-L-alanine
  • (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-furan-2-ylpropanoate
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