CAS 167262-69-3

1-Piperidinecarboxylic acid, 4-(aminocarbonyl)-4-phenyl-, 1,1-dimethylethyl ester

Description:

1-Piperidinecarboxylic acid, 4-(aminocarbonyl)-4-phenyl-, 1,1-dimethylethyl ester, commonly referred to by its CAS number 167262-69-3, is a chemical compound characterized by its piperidine ring structure, which contributes to its basicity and potential for forming hydrogen bonds. This compound features a carboxylic acid moiety that is esterified with a tert-butyl group, enhancing its lipophilicity and stability. The presence of an aminocarbonyl group and a phenyl substituent indicates potential for various interactions, including aromatic stacking and dipole-dipole interactions. Its molecular structure suggests it may exhibit biological activity, possibly as a pharmaceutical intermediate or active ingredient. The compound's solubility, reactivity, and stability can be influenced by the functional groups present, making it of interest in medicinal chemistry and organic synthesis. As with many organic compounds, safety data and handling precautions should be considered, particularly regarding its potential toxicity and environmental impact.

Formula: C₁₇H₂₄N₂O₃

InChI: InChI=1S/C17H24N2O3/c1-16(2,3)22-15(21)19-11-9-17(10-12-19,14(18)20)13-7-5-4-6-8-13/h4-8H,9-12H2,1-3H3,(H2,18,20)

InChI key: InChIKey=YFFNTRHCIKUMCA-UHFFFAOYSA-N

SMILES: C(N)(=O)C1(CCN(C(OC(C)(C)C)=O)CC1)C2=CC=CC=C2

Synonyms:

• 1-Piperidinecarboxylic acid, 4-(aminocarbonyl)-4-phenyl-, 1,1-dimethylethyl ester

tert-Butyl 4-carbamoyl-4-phenylpiperidine-1-carboxylate

CAS: 167262-69-3

tert-Butyl 4-carbamoyl-4-phenylpiperidine-1-carboxylate

Molecular weight: 304.38g/mol

Ref: 54-OR310513