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Atomfair Ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate C16H20N2O2

Description Ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate (CAS No. 123730-67-6) is a high-purity synthetic organic compound with the molecular formula C16H20N2O2. This piperidine derivative features a benzyl group at the 1-position, a cyano group at the 4-position, and an ethyl ester moiety, making it a versatile intermediate for pharmaceutical and chemical research. Its well-defined structure (IUPAC name: ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate) ensures reproducibility in synthetic applications. Suitable for use in medicinal chemistry, this compound is provided as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for quality assurance. Store in a cool, dry place under inert conditions to maintain stability.

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Description

Description

Ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate (CAS No. 123730-67-6) is a high-purity synthetic organic compound with the molecular formula C16H20N2O2. This piperidine derivative features a benzyl group at the 1-position, a cyano group at the 4-position, and an ethyl ester moiety, making it a versatile intermediate for pharmaceutical and chemical research. Its well-defined structure (IUPAC name: ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate) ensures reproducibility in synthetic applications. Suitable for use in medicinal chemistry, this compound is provided as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for quality assurance. Store in a cool, dry place under inert conditions to maintain stability.

  • CAS No: 123730-67-6
  • Molecular Formula: C16H20N2O2
  • Molecular Weight: 272.34
  • Exact Mass: 272.152477885
  • Monoisotopic Mass: 272.152477885
  • IUPAC Name: ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate
  • SMILES: CCOC(=O)C1(CCN(CC1)CC2=CC=CC=C2)C#N
  • Synonyms: 123730-67-6, ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate, DTXSID50558581, DTXCID60509362, 963-060-5

Application

Ethyl 1-benzyl-4-cyanopiperidine-4-carboxylate is a key intermediate in the synthesis of biologically active piperidine derivatives, particularly in CNS-targeting drug discovery. Its functional groups enable further modifications, such as hydrolysis or reduction, to access novel pharmacophores. Researchers utilize this compound in the development of potential neuropharmaceuticals due to its structural resemblance to neurotransmitter modulators. It is also employed in scaffold diversification for high-throughput screening libraries.

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