CAS 318279-38-8
:3-Piperidinemethanol,4-(4-fluorophenyl)-1-methyl-
Description:
3-Piperidinemethanol, 4-(4-fluorophenyl)-1-methyl- is a chemical compound characterized by its piperidine ring structure, which is a six-membered ring containing one nitrogen atom. This compound features a hydroxymethyl group (-CH2OH) attached to the piperidine nitrogen, enhancing its potential for hydrogen bonding and solubility in polar solvents. The presence of a 4-fluorophenyl group indicates that there is a fluorine atom substituted on a phenyl ring, which can influence the compound's electronic properties and biological activity. The methyl group at the 1-position of the piperidine ring contributes to its steric and electronic characteristics. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas targeting central nervous system disorders. As with many organic compounds, its stability, reactivity, and interactions with biological systems would depend on various factors, including pH, temperature, and the presence of other chemical entities.
Formula:C13H18FNO
Synonyms:- (+/-)-Trans-4-(4-Fluorophenyl)-3-Hydroxymethyl-1-Methylpiperidine
- (+/-)-Trans-4-(Fluorophenyl)-3-Hydroxymethyl-1-Methylpiperidine
- Trans-4-(P-Fluorophenyl)-3-Hydroxymethyl-1-Methylpiperidine
- (3R-,4S)-Rel-4-(4-Fluorophenyl)-1-Methyl-3-Piperidine Methanol
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Found 3 products.
trans-4-(4-Fluorophenyl)-3-hydroxymethyl-1-methylpiperidine
CAS:<p>The compound is a natural product and its structure is similar to that of the neurotransmitter dopamine. The compound has been used in pharmacological studies as a tool for understanding the neurotoxicity of dopamine and other drugs. This drug has also been used to investigate the level of dopamine receptor occupancy by various dopaminergic drugs.</p>Formula:C13H18FNOPurity:Min. 95%Molecular weight:223.29 g/molRef: 4Z-P-0252
Discontinued product

