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CAS 103321-52-4

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9H-Fluoren-9-ylmethyl (2S)-2-(chlorocarbonyl)-1-pyrrolidinecarboxylate

Description:
9H-Fluoren-9-ylmethyl (2S)-2-(chlorocarbonyl)-1-pyrrolidinecarboxylate is a chemical compound characterized by its complex structure, which includes a fluorenylmethyl group and a pyrrolidine ring with a chlorocarbonyl substituent. This compound typically exhibits properties associated with both aromatic and aliphatic systems, contributing to its potential reactivity and stability. The presence of the chlorocarbonyl group suggests that it may participate in nucleophilic acyl substitution reactions, making it a useful intermediate in organic synthesis. The chirality at the pyrrolidine carbon indicates that it may exhibit stereochemical properties, which can influence its biological activity and interactions. Additionally, the fluorenylmethyl moiety can enhance lipophilicity, potentially affecting the compound's solubility and permeability in biological systems. Overall, this compound's unique structural features make it of interest in medicinal chemistry and synthetic organic chemistry, particularly in the development of pharmaceuticals or agrochemicals.
Formula:C20H18ClNO3
InChI:InChI=1S/C20H18ClNO3/c21-19(23)18-10-5-11-22(18)20(24)25-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2/t18-/m0/s1
InChI key:InChIKey=DKNLJWSDGPXALN-SFHVURJKSA-N
SMILES:C(OC(=O)N1[C@H](C(Cl)=O)CCC1)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:
  • N-(9-Fluorenylmethoxycarbonyl)prolyl chloride
  • FMOC-PRO-CL
  • 1-Pyrrolidinecarboxylic acid, 2-(chlorocarbonyl)-, 9H-fluoren-9-ylmethyl ester, (S)-
  • NALPHA-9-Fluorenylmethoxycarbonyl-L-prolyl chloride
  • 1-Pyrrolidinecarboxylic acid, 2-(chlorocarbonyl)-, 9H-fluoren-9-ylmethyl ester, (2S)-
  • 9H-Fluoren-9-ylmethyl (2S)-2-(chlorocarbonyl)-1-pyrrolidinecarboxylate
  • Fmoc-L-Pro-Cl
  • FMOC-L-PROLYL CHLORIDE
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