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CAS 269726-95-6

:

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

Description:
(3R)-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 and peptides. The Fmoc group serves as a protective moiety for the amino group, allowing for selective reactions during the synthesis process. The presence of the hexenoic acid moiety introduces unsaturation, which can influence the compound's reactivity and properties. Additionally, the stereochemistry at the 3-position (designated as (3R)) indicates that the compound has a specific three-dimensional arrangement, which can affect its biological activity and interactions. Overall, this compound is significant in the field of organic chemistry and biochemistry, particularly in the development of pharmaceuticals and biologically active molecules.
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-/m1/s1
InChI key:InChIKey=SVCMPCVPSYAVJO-CQSZACIVSA-N
SMILES:C(OC(N[C@@H](CC(O)=O)CC=C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • (3R)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-5-hexenoic acid
  • (3R)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hex-5-enoic acid
  • 5-Hexenoic acid, 3-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (3R)-
  • Fmoc-D-β-HoGly(Allyl)-OH
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