4-FLUORO-4-HYDROXYMETHYL-1-METHYLPIPERIDINE
Names and Identifiers of 1000341-04-7
CAS Number |
1000341-04-7 |
|---|---|
MDL Number |
MFCD09880180 |
IUPAC Name |
(4-fluoro-1-methylpiperidin-4-yl)methanol |
InChI |
InChI=1S/C7H14FNO/c1-9-4-2-7(8,6-10)3-5-9/h10H,2-6H2,1H3 |
InChIKey |
ZACQKYSISKMVCF-UHFFFAOYSA-N |
Canonical SMILES |
CN1CCC(F)(CO)CC1 |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000341-04-7
Exact Mass |
147.10600 |
|---|---|
LogP |
0.35050 |
Molecular Formula |
C7H14FNO |
Molecular Weight |
147.19100 |
PSA |
23.47000 |
Safety Information of 1000341-04-7
Applications of 1000341-04-7
The applications of 4-fluoro-1-methyl-4-piperidinemethanol span several fields:
- Pharmaceuticals: Due to its potential biological activity, it may serve as a lead compound in drug development for neurological disorders.
- Chemical Research: It is utilized in synthetic organic chemistry as an intermediate for producing other complex molecules.
- Material Science: Its unique properties may be explored in developing new materials or coatings with specific functionalities.
Interaction Studies of 1000341-04-7
Interaction studies involving 4-fluoro-1-methyl-4-piperidinemethanol focus on its binding affinity to various biological targets, particularly neurotransmitter receptors. These studies aim to elucidate its mechanism of action and potential therapeutic effects. Preliminary data suggest that its fluorinated structure may enhance interactions with certain receptors compared to non-fluorinated analogs.
Biological Activity of 1000341-04-7
Research indicates that compounds containing piperidine rings exhibit diverse biological activities, including analgesic, antidepressant, and anti-inflammatory effects. Specifically, 4-fluoro-1-methyl-4-piperidinemethanol has shown potential in pharmacological studies related to its structural similarity to known psychoactive substances. Its fluorinated structure may enhance lipophilicity, potentially increasing bioavailability and central nervous system penetration.