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CAS 1311992-98-9

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2-but-3-enyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)hex-5-enoic acid

Description:
2-but-3-enyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)hex-5-enoic acid is a complex organic compound characterized by its unique structural features, which include multiple functional groups and a conjugated system. This compound contains an amino acid backbone with a fluorenylmethoxycarbonyl (Fmoc) protecting group, commonly used in peptide synthesis to protect the amino group during reactions. The presence of double bonds in the butenyl and hexenoic acid portions contributes to its reactivity and potential applications in organic synthesis. The compound's molecular structure suggests it may exhibit interesting properties such as UV absorbance due to the aromatic fluorenyl group, which can be useful in various analytical techniques. Additionally, the presence of the carboxylic acid functional group indicates potential for hydrogen bonding and solubility in polar solvents. Overall, this compound's characteristics make it a valuable intermediate in the synthesis of more complex molecules, particularly in the fields of medicinal chemistry and materials science.
Formula:C25H27NO4
InChI:InChI=1S/C25H27NO4/c1-3-5-15-25(23(27)28,16-6-4-2)26-24(29)30-17-22-20-13-9-7-11-18(20)19-12-8-10-14-21(19)22/h3-4,7-14,22H,1-2,5-6,15-17H2,(H,26,29)(H,27,28)
SMILES:C=CCCC(CCC=C)(C(=O)O)N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:
  • 5-Hexenoic acid, 2-(3-buten-1-yl)-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-
  • N-FMoc-2-amino-2-(3-butenyl)hex-5-enoic acid
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