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CAS 288617-72-1

:

(2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-5-hexenoic acid

Description:
(2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-5-hexenoic acid, with CAS number 288617-72-1, is a synthetic organic compound that features a unique structure characterized by a hexenoic acid backbone. This compound contains a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis to protect amino groups during the formation of peptide bonds. The presence of the double bond in the hexenoic acid portion contributes to its reactivity and potential applications in organic synthesis. The stereochemistry at the 2-position is specified as (2S), indicating that it has a specific spatial arrangement that can influence its biological activity and interactions. This compound is typically utilized in the field of medicinal chemistry and peptide synthesis, where the Fmoc group allows for selective deprotection and subsequent reactions. Its characteristics, including solubility and stability, may vary depending on the solvent and conditions used in experiments. Overall, this compound serves as a valuable intermediate in the synthesis of more complex molecules.
Formula:C22H23NO4
InChI:InChI=1S/C22H23NO4/c1-3-4-13-22(2,20(24)25)23-21(26)27-14-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h3,5-12,19H,1,4,13-14H2,2H3,(H,23,26)(H,24,25)/t22-/m0/s1
InChI key:InChIKey=ZZWOKVRONYEEBJ-QFIPXVFZSA-N
SMILES:C(OC(N[C@@](CCC=C)(C(O)=O)C)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:
  • (2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-5-hexenoic acid
  • (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methylhex-5-enoic acid
  • (S)-N-Fmoc-2-(3'-butenyl)alanine
  • 5-Hexenoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-2-methyl-, (2S)-
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