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CAS 270263-04-2

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(3S)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-5-hexenoic acid

Description:
(3S)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-5-hexenoic acid is a synthetic organic compound characterized by its unique structure, which includes a hexenoic acid backbone and a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound is typically used in peptide synthesis as a building block, particularly in the formation of amino acids. The Fmoc group serves as a protective moiety for the amino group, allowing for selective reactions during peptide assembly. The presence of the hexenoic acid moiety introduces unsaturation, which can influence the compound's reactivity and properties. The stereochemistry at the 3-position is crucial for its biological activity and interaction with other molecules. This compound is soluble in organic solvents, and its stability can be affected by factors such as pH and temperature. Overall, (3S)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-5-hexenoic acid is an important intermediate in the field of organic synthesis and medicinal chemistry, particularly in the development of peptide-based therapeutics.
Formula:C21H21NO4
InChI:InChI=1S/C21H21NO4/c1-2-7-14(12-20(23)24)22-21(25)26-13-19-17-10-5-3-8-15(17)16-9-4-6-11-18(16)19/h2-6,8-11,14,19H,1,7,12-13H2,(H,22,25)(H,23,24)/t14-/m0/s1
InChI key:InChIKey=SVCMPCVPSYAVJO-AWEZNQCLSA-N
SMILES:C(OC(N[C@H](CC(O)=O)CC=C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • (3S)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-5-hexenoic acid
  • (3S)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hex-5-enoic acid
  • 5-Hexenoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (3S)-
  • Fmoc-β-HoGly(Allyl)-OH
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