CAS 916421-12-0

1,1-Dimethylethyl 3-amino-4-(3-fluorophenyl)-1-piperidinecarboxylate

Description:

1,1-Dimethylethyl 3-amino-4-(3-fluorophenyl)-1-piperidinecarboxylate, identified by its CAS number 916421-12-0, is a chemical compound characterized by its piperidine structure, which includes a carboxylate functional group and an amino group. The presence of a 3-fluorophenyl substituent indicates that it has a fluorine atom attached to a phenyl ring, contributing to its potential biological activity and lipophilicity. The dimethyl group at the 1-position of the piperidine ring enhances steric hindrance, which may influence the compound's interaction with biological targets. This compound is likely to exhibit properties typical of piperidine derivatives, such as potential use in medicinal chemistry for developing pharmaceuticals. Its specific characteristics, including solubility, stability, and reactivity, would depend on the molecular interactions dictated by its functional groups and overall structure. As with many compounds in this class, it may be of interest for its pharmacological properties, particularly in the context of drug design and development.

Formula: C₁₆H₂₃FN₂O₂

InChI: InChI=1S/C16H23FN2O2/c1-16(2,3)21-15(20)19-8-7-13(14(18)10-19)11-5-4-6-12(17)9-11/h4-6,9,13-14H,7-8,10,18H2,1-3H3

InChI key: InChIKey=FYDLKIMTIIGWBV-UHFFFAOYSA-N

SMILES: NC1C(C2=CC(F)=CC=C2)CCN(C(OC(C)(C)C)=O)C1

Synonyms:

• 1,1-Dimethylethyl 3-amino-4-(3-fluorophenyl)-1-piperidinecarboxylate
• tert-Butyl 3-amino-4-(3-fluorophenyl)piperidine-1-carboxylate
• 1-Piperidinecarboxylic acid, 3-amino-4-(3-fluorophenyl)-, 1,1-dimethylethyl ester