CAS 1858257-30-3

Ethyl 1-(5-methyl-6-phenylthieno[2,3-d]pyrimidin-4-yl)-4-piperidinecarboxylate

Description:

Ethyl 1-(5-methyl-6-phenylthieno[2,3-d]pyrimidin-4-yl)-4-piperidinecarboxylate is a chemical compound characterized by its complex structure, which includes a thieno[2,3-d]pyrimidine core, a piperidine ring, and an ethyl ester functional group. This compound is likely to exhibit properties typical of heterocyclic compounds, including potential biological activity due to the presence of the thieno and pyrimidine moieties, which are often associated with pharmacological effects. The piperidine ring contributes to its basicity and may influence its solubility and reactivity. The presence of the phenyl group suggests potential for π-π interactions, which can affect the compound's interactions with biological targets. Additionally, the methyl group on the thieno-pyrimidine structure may influence steric and electronic properties, impacting its overall reactivity and stability. As a compound of interest in medicinal chemistry, it may be evaluated for its potential therapeutic applications, although specific biological activity and safety profiles would require further investigation through experimental studies.

Formula: C₂₁H₂₃N₃O₂S

InChI: InChI=1S/C21H23N3O2S/c1-3-26-21(25)16-9-11-24(12-10-16)19-17-14(2)18(15-7-5-4-6-8-15)27-20(17)23-13-22-19/h4-8,13,16H,3,9-12H2,1-2H3

InChI key: InChIKey=CDOBSFZBBYYMOP-UHFFFAOYSA-N

SMILES: CC=1C2=C(N=CN=C2SC1C3=CC=CC=C3)N4CCC(C(OCC)=O)CC4

Synonyms:

• Ethyl 1-(5-methyl-6-phenylthieno[2,3-d]pyrimidin-4-yl)-4-piperidinecarboxylate
• 4-Piperidinecarboxylic acid, 1-(5-methyl-6-phenylthieno[2,3-d]pyrimidin-4-yl)-, ethyl ester
• Ethyl 1-(5-methyl-6-phenylthieno[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylate

Ethyl 1-(5-methyl-6-phenylthieno[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylate

CAS: 1858257-30-3

Ethyl 1-(5-methyl-6-phenylthieno[2,3-d]pyrimidin-4-yl)piperidine-4-carboxylate

Purity: ≥95%

Molecular weight: 381.49g/mol

Ref: 54-OR111064