CAS 1286266-09-8

1,1-Dimethylethyl N-[1-[(4-bromophenyl)methyl]-4-piperidinyl]carbamate

Description:

1,1-Dimethylethyl N-[1-[(4-bromophenyl)methyl]-4-piperidinyl]carbamate, identified by its CAS number 1286266-09-8, is a chemical compound characterized by its complex structure, which includes a carbamate functional group and a piperidine ring. This substance typically exhibits properties associated with both lipophilicity and hydrophilicity due to the presence of various functional groups, making it potentially soluble in organic solvents while having some degree of solubility in polar solvents. The bromophenyl moiety may impart specific electronic and steric effects, influencing its reactivity and interaction with biological targets. As a carbamate, it may also exhibit characteristics typical of this class, such as potential inhibition of certain enzymes or receptors. The compound's molecular structure suggests it could be of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting neurological or other biological pathways. However, detailed studies would be necessary to fully elucidate its biological activity, toxicity, and potential applications.

Formula: C₁₇H₂₅BrN₂O₂

InChI: InChI=1S/C17H25BrN2O2/c1-17(2,3)22-16(21)19-15-8-10-20(11-9-15)12-13-4-6-14(18)7-5-13/h4-7,15H,8-12H2,1-3H3,(H,19,21)

InChI key: InChIKey=DROWWMOQDRCQGK-UHFFFAOYSA-N

SMILES: C(N1CCC(NC(OC(C)(C)C)=O)CC1)C2=CC=C(Br)C=C2

Synonyms:

• Carbamic acid, N-[1-[(4-bromophenyl)methyl]-4-piperidinyl]-, 1,1-dimethylethyl ester
• 1,1-Dimethylethyl N-[1-[(4-bromophenyl)methyl]-4-piperidinyl]carbamate
• [1-(4-Bromo-benzyl)-piperidin-4-yl]-carbamic acid tert-butyl ester
• tert-Butyl 1-(4-bromobenzyl)piperidin-4-ylcarbamate