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CAS 672310-11-1

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(9H-fluoren-9-yl)methyl3-oxopiperidine-1-carboxylate

Description:
(9H-fluoren-9-yl)methyl 3-oxopiperidine-1-carboxylate is a chemical compound characterized by its unique structure, which includes a fluorenyl group and a piperidine ring. The presence of the fluorenyl moiety contributes to its aromatic properties, while the piperidine ring introduces a cyclic amine structure, which can influence its reactivity and biological activity. This compound typically exhibits moderate to high lipophilicity due to the aromatic system, which may affect its solubility in organic solvents and its permeability through biological membranes. The ester functional group in the carboxylate portion can undergo hydrolysis, making it reactive under certain conditions. Additionally, the ketone group in the piperidine ring can participate in various chemical reactions, such as nucleophilic attacks. Overall, this compound may have potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological targets. However, specific biological activity and safety profiles would require further investigation through experimental studies.
Formula:C20H19NO3
InChI:InChI=1/C20H19NO3/c22-14-6-5-11-21(12-14)20(23)24-13-19-17-9-3-1-7-15(17)16-8-2-4-10-18(16)19/h1-4,7-10,19H,5-6,11-13H2
SMILES:c1ccc2c(c1)c1ccccc1C2COC(=O)N1CCCC(=O)C1
Synonyms:
  • 1-Piperidinecarboxylic acid, 3-oxo-, 9H-fluoren-9-ylmethyl ester
  • 9H-Fluoren-9-ylmethyl 3-oxopiperidine-1-carboxylate
  • 1-N-Fmoc-3-Piperidone
  • 1-FMOC-3-piperidinone
  • (9H-Fluoren-9-yl)methyl 3-oxopiperidine-1-carboxylate
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