structure of 2-(3-Fluoro-5-methylphenyl)ethan-1-ol

2-(3-Fluoro-5-methylphenyl)ethan-1-ol

CAS No.: 1000534-18-8
M. Wt: 154.18100
M. Fa: C9H11FO
InChI Key: OTILJLHCRMORIH-UHFFFAOYSA-N

Names and Identifiers of 2-(3-Fluoro-5-methylphenyl)ethan-1-ol

CAS Number

1000534-18-8

MDL Number

MFCD09926457

IUPAC Name

2-(3-fluoro-5-methylphenyl)ethanol

InChI

InChI=1S/C9H11FO/c1-7-4-8(2-3-11)6-9(10)5-7/h4-6,11H,2-3H2,1H3

InChIKey

OTILJLHCRMORIH-UHFFFAOYSA-N

Canonical SMILES

CC1=CC(=CC(=C1)F)CCO

UNSPSC Code

12352100

Physical and chemical properties of 2-(3-Fluoro-5-methylphenyl)ethan-1-ol

Acidity coefficient

14.76±0.10(Predicted)

Boiling Point

226.4±25.0 °C(Predicted)

Density

1.099±0.06 g/cm3(Predicted)

Exact Mass

154.07900

LogP

1.66890

Molecular Formula

C9H11FO

Molecular Weight

154.18100

PSA

20.23000

Safety Information of 2-(3-Fluoro-5-methylphenyl)ethan-1-ol

Pictograms

Signal Word

Warning

Safety Data Sheet

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

Applications of 2-(3-Fluoro-5-methylphenyl)ethan-1-ol

2-(3-Fluoro-5-methylphenyl)ethanol has several applications across different fields:

  • Pharmaceuticals: It serves as an intermediate in the synthesis of various drugs targeting specific diseases.
  • Agrochemicals: Utilized in the development of agricultural chemicals.
  • Specialty Chemicals: Employed in the production of specialty chemicals and materials due to its unique properties.

Interaction Studies of 2-(3-Fluoro-5-methylphenyl)ethan-1-ol

Studies on the interactions of 2-(3-fluoro-5-methylphenyl)ethanol with biological systems have indicated its potential role in modulating enzyme activity and receptor interactions. The compound's ability to form hydrogen bonds due to its hydroxyl group enhances its interaction with various molecular targets, which is crucial for its biological effects.

Biological Activity of 2-(3-Fluoro-5-methylphenyl)ethan-1-ol

Research indicates that 2-(3-fluoro-5-methylphenyl)ethanol exhibits potential biological activities. It has been studied for its antimicrobial and anti-inflammatory properties, suggesting that it may interact with specific biological targets, potentially inhibiting certain enzymes or receptors. The exact mechanisms of action depend on the context of use and the specific biological systems involved.