162648-31-9

Basic information

• Product Name: 1-Benzoyl-4-methyl-piperidine-4-carboxylic acid
• Synonyms: 1-Benzoyl-4-methyl-piperidine-4-carboxylic acid
• CAS NO: 162648-31-9
• Molecular Weight: 247.294
• Mol File: 162648-31-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Benzoyl-4-methyl-piperidine-4-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Benzoyl-4-methyl-piperidine-4-carboxylic acid(162648-31-9)
• EPA Substance Registry System: 1-Benzoyl-4-methyl-piperidine-4-carboxylic acid(162648-31-9)

Safety Data

• Hazardous Substances Data: 162648-31-9(Hazardous Substances Data)

Usage

Abbreviation

BMPC

Type of compound

Chemical compound

Derivative of

Piperidine

Functional groups

Benzoyl and carboxylic acid

Psychoactive substance

Yes

Receptor interaction

Potent and selective agonist at the dopamine D3 receptor

Potential applications

Treatment of neuropsychiatric disorders (e.g., schizophrenia, drug addiction), Parkinson's disease, and other movement disorders

Research use

Neuroscience studies to understand dopamine receptor mechanisms in the brain

Upstream product

• 1126-09-6 4-carbethoxypiperidine 
• 98-88-4 benzoyl chloride 
• 136081-74-8 ethyl 1-benzoyl-4-piperidine-carboxylate 
• 162648-30-8 1-benzoyl-4-methylpiperidine-4-carboxylic acid ethyl ester 
• 498-94-2 isonipecotic acid 
• 5274-99-7 1-benzoylisonipecotic acid 

Downstream Products

• 1383116-17-3 (4-fluoro-4-methylpiperidin-1-yl)(phenyl)methanone 
• 163271-08-7 4-tert-butoxycarbonylamino-4-methylpiperidine 
• 1262787-56-3 (1-benzoyl-4-methylpiperidin-4-yl)carbamic acid tert-butyl ester 
• 162648-32-0 4-methylpiperidine-4-carboxylic acid 

Relevant articles and documents

Decarboxylative fluorination of aliphatic carboxylic acids via photoredox catalysis

The direct conversion of aliphatic carboxylic acids to the corresponding alkyl fluorides has been achieved via visible light-promoted photoredox catalysis. This operationally simple, redox-neutral fluorination method is amenable to a wide variety of carboxylic acids. Photon-induced oxidation of carboxylates leads to the formation of carboxyl radicals, which upon rapid CO2-extrusion and F? transfer from a fluorinating reagent yield the desired fluoroalkanes with high efficiency. Experimental evidence indicates that an oxidative quenching pathway is operable in this broadly applicable fluorination protocol.

Hindered esters of rapamycin

A compound of the structure STR1 wherein R and R1 are each, independently, STR2 or hydrogen; R2 and R3 are each, independently, alkyl, arylalkyl, or R2 and R3 may be taken together to form a cycloalky