structure of Benzeneethanol, 3-fluoro-4-(trifluoromethyl)-

Benzeneethanol, 3-fluoro-4-(trifluoromethyl)-

CAS No.: 1000560-90-6
M. Wt: 208.15
M. Fa: C9H8F4O
InChI Key: IVAIIWIJJRTLNY-UHFFFAOYSA-N

Names and Identifiers of 1000560-90-6

CAS Number

1000560-90-6

MDL Number

MFCD09926434

IUPAC Name

2-[3-fluoro-4-(trifluoromethyl)phenyl]ethanol

InChI

InChI=1S/C9H8F4O/c10-8-5-6(3-4-14)1-2-7(8)9(11,12)13/h1-2,5,14H,3-4H2

InChIKey

IVAIIWIJJRTLNY-UHFFFAOYSA-N

Canonical SMILES

C1=CC(=C(C=C1CCO)F)C(F)(F)F

UNSPSC Code

12352100

Physical and chemical properties of 1000560-90-6

Boiling Point

222.0±35.0 °C(Predicted)

Density

1.321±0.06 g/cm3(Predicted)

H Bond Acceptors

1

H Bond Donors

1

LogP

2.51510767166667

Molecular Formula

C9H8F4O

Molecular Weight

208.15

Safety Information of 1000560-90-6

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of 1000560-90-6

Benzeneethanol, 3-fluoro-4-(trifluoromethyl)- has diverse applications in:

  • Pharmaceuticals: Used as an intermediate in the synthesis of various drugs due to its unique chemical properties.
  • Agricultural Chemicals: Potential applications in developing agrochemicals that require specific bioactivity.
  • Research: Employed in scientific studies to explore its biological effects and interactions with other compounds.

Interaction Studies of 1000560-90-6

Interaction studies involving benzeneethanol, 3-fluoro-4-(trifluoromethyl)- focus on its binding affinity with biological targets such as enzymes and receptors. Research indicates that fluorinated compounds often exhibit altered interaction profiles compared to their non-fluorinated counterparts. These studies are essential for understanding the compound's potential therapeutic roles and mechanisms of action.

Biological Activity of 1000560-90-6

Research indicates that benzeneethanol derivatives exhibit significant biological activities, including antimicrobial and anti-inflammatory properties. The presence of fluorine atoms often enhances the lipophilicity of these compounds, potentially increasing their bioavailability and efficacy in biological systems. Specific studies have shown that compounds with similar structures can inhibit certain enzymes or act as receptor modulators, suggesting that benzeneethanol, 3-fluoro-4-(trifluoromethyl)- may also possess such activities.