structure of 2-Pyridineethanol, 5-fluoro-

2-Pyridineethanol, 5-fluoro-

CAS No.: 1000521-75-4
M. Wt: 141.14300
M. Fa: C7H8FNO
InChI Key: OVQRVQOBZKDTQQ-UHFFFAOYSA-N
Appearance: yellow liquid

Names and Identifiers of 2-Pyridineethanol, 5-fluoro-

CAS Number

1000521-75-4

MDL Number

MFCD09926281

IUPAC Name

2-(5-fluoropyridin-2-yl)ethanol

InChI

InChI=1S/C7H8FNO/c8-6-1-2-7(3-4-10)9-5-6/h1-2,5,10H,3-4H2

InChIKey

OVQRVQOBZKDTQQ-UHFFFAOYSA-N

Canonical SMILES

C1=CC(=NC=C1F)CCO

UNSPSC Code

12352100

Physical and chemical properties of 2-Pyridineethanol, 5-fluoro-

Acidity coefficient

14.36±0.10(Predicted)

Boiling Point

210.6±25.0 °C(Predicted)

Density

1.204±0.06 g/cm3(Predicted)

Exact Mass

141.05900

H Bond Acceptors

2

H Bond Donors

1

LogP

0.75550

Molecular Formula

C7H8FNO

Molecular Weight

141.14300

PSA

33.12000

Safety Information of 2-Pyridineethanol, 5-fluoro-

Pictograms

Signal Word

 Danger

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

Applications of 2-Pyridineethanol, 5-fluoro-

The applications of 2-(5-Fluoropyridin-2-yl)ethan-1-ol span several fields:

  • Medicinal Chemistry: It is explored as a potential drug candidate due to its bioactive properties.
  • Material Science: The compound is used in developing advanced materials with enhanced thermal stability and chemical resistance.
  • Organic Synthesis: It serves as a versatile building block for synthesizing more complex fluorinated compounds.

Interaction Studies of 2-Pyridineethanol, 5-fluoro-

Studies focusing on the interactions of 2-(5-Fluoropyridin-2-yl)ethan-1-ol with biological systems reveal its potential effects on cellular signaling pathways. Its ability to form strong hydrogen bonds and engage in π–π interactions with receptors enhances its efficacy as a modulator of biological activity. This interaction profile is critical for understanding its mechanism of action and optimizing its pharmacological properties.

Biological Activity of 2-Pyridineethanol, 5-fluoro-

Research indicates that 2-(5-Fluoropyridin-2-yl)ethan-1-ol exhibits significant biological activity, particularly in pharmacological contexts. Its interaction with various biological targets suggests potential applications in treating neurological disorders, due to its ability to modulate neurotransmitter systems. Studies have shown that compounds containing the 5-fluoropyridine moiety often display antimicrobial and anticancer properties, making this compound a candidate for further investigation in drug development.