2-(5-Fluoro-2-methoxyphenyl)ethanol
CAS No.:
1000571-93-6
M. Wt:
170.18
M. Fa:
C9H11FO2
InChI Key:
RZLJHDVEADCDNS-UHFFFAOYSA-N
Names and Identifiers of 2-(5-Fluoro-2-methoxyphenyl)ethanol
CAS Number |
1000571-93-6 |
|---|---|
MDL Number |
MFCD09926212 |
IUPAC Name |
2-(5-fluoro-2-methoxyphenyl)ethanol |
InChI |
InChI=1S/C9H11FO2/c1-12-9-3-2-8(10)6-7(9)4-5-11/h2-3,6,11H,4-5H2,1H3 |
InChIKey |
RZLJHDVEADCDNS-UHFFFAOYSA-N |
Canonical SMILES |
COC1=C(C=C(C=C1)F)CCO |
UNSPSC Code |
12352100 |
Physical and chemical properties of 2-(5-Fluoro-2-methoxyphenyl)ethanol
Molecular Formula |
C9H11FO2 |
|---|---|
Molecular Weight |
170.18 |
Safety Information of 2-(5-Fluoro-2-methoxyphenyl)ethanol
Applications of 2-(5-Fluoro-2-methoxyphenyl)ethanol
2-(5-Fluoro-2-methoxyphenyl)ethanol has several applications across various fields:
- Pharmaceutical Research: Investigated for its potential as an antimicrobial and anticancer agent.
- Chemical Synthesis: Serves as an intermediate in the synthesis of more complex organic molecules.
- Material Science: May be explored for its properties in creating new materials due to its unique chemical structure.
Biological Activity of 2-(5-Fluoro-2-methoxyphenyl)ethanol
Research indicates that 2-(5-Fluoro-2-methoxyphenyl)ethanol exhibits potential biological activity, particularly in antimicrobial and anticancer studies. Its unique structure allows it to interact with specific biological targets, potentially modulating enzyme activity or receptor interactions. Fluorinated compounds often demonstrate enhanced lipophilicity, improving cellular uptake and bioavailability, which may contribute to their biological effectiveness.
