CAS 182223-53-6

benzyl (1-benzylpiperidin-4-yl)carbamate

Description:

Benzyl (1-benzylpiperidin-4-yl)carbamate, identified by its CAS number 182223-53-6, is a chemical compound characterized by its unique structure, which includes a piperidine ring substituted with benzyl groups and a carbamate functional group. This compound typically exhibits properties associated with both piperidine derivatives and carbamates, such as potential biological activity and solubility in organic solvents. The presence of the benzyl groups may enhance lipophilicity, influencing its interaction with biological membranes and receptors. As a carbamate, it may also exhibit characteristics typical of this functional group, such as susceptibility to hydrolysis under certain conditions. The compound's potential applications could span various fields, including medicinal chemistry, where it may serve as a lead compound for drug development or as a tool in biochemical research. However, specific details regarding its reactivity, stability, and biological effects would require further investigation through empirical studies and literature review.

Formula: C₂₀H₂₄N₂O₂

InChI: InChI=1/C20H24N2O2/c23-20(24-16-18-9-5-2-6-10-18)21-19-11-13-22(14-12-19)15-17-7-3-1-4-8-17/h1-10,19H,11-16H2,(H,21,23)

SMILES: c1ccc(cc1)CN1CCC(CC1)N=C(O)OCc1ccccc1

Carbamic acid, [1-(phenylmethyl)-4-piperidinyl]-, phenylmethyl ester (9CI)

CAS: 182223-53-6

Formula: C₂₀H₂₄N₂O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 324.4168

Ref: IN-DA0023HW

1-Benzyl-4-benzyloxycarbonylaminopiperidine

Controlled Product

CAS: 182223-53-6

Applications Intermediate used in the preparation p-38 kinase inhibitors and serotonin antagonists.
References Schaus, J.M., et al.: J. Med. Chem., 41, 1943 (1998),

Formula: C₂₀H₂₄N₂O₂

Color and Shape: Neat

Molecular weight: 324.42

Ref: TR-B232660