structure of 2,5-Pyridinediethanol

2,5-Pyridinediethanol

CAS No.: 1000571-88-9
M. Wt: 167.205
M. Fa: C9H13NO2
InChI Key: -

Names and Identifiers of 2,5-Pyridinediethanol

CAS Number

1000571-88-9

IUPAC Name

2-[6-(2-hydroxyethyl)pyridin-3-yl]ethanol

Canonical SMILES

C1=CC(=NC=C1CCO)CCO

Physical and chemical properties of 2,5-Pyridinediethanol

Boiling Point

328.8±32.0 °C at 760 mmHg

Density

1.2±0.1 g/cm3

Exact Mass

167.094635

Flash Point

152.6±25.1 °C

Index of Refraction

1.563

LogP

-0.99

Molecular Formula

C9H13NO2

Molecular Weight

167.205

Vapour Pressure

0.0±0.8 mmHg at 25°C

Applications of 2,5-Pyridinediethanol

The applications of 2,5-Pyridinediethanol span various industries:

  • Pharmaceuticals: Due to its biological activity, it may serve as a precursor or intermediate in drug development.
  • Chemical Synthesis: It can be used as a building block in organic synthesis for creating more complex molecules.
  • Agricultural Chemicals: Potential use in developing agrochemicals that require specific biological activity.

Its unique properties make it valuable across multiple fields.

Interaction Studies of 2,5-Pyridinediethanol

Interaction studies involving 2,5-Pyridinediethanol often focus on its behavior with other biological molecules or its interaction with receptors. These studies help elucidate:

  • Binding Affinity: Understanding how well the compound binds to specific targets can inform its potential therapeutic uses.
  • Synergistic Effects: Investigating how it interacts with other drugs may reveal enhanced efficacy or reduced side effects when used in combination therapies.

Such studies are crucial for advancing its application in medicine.

Biological Activity of 2,5-Pyridinediethanol

2,5-Pyridinediethanol has been studied for its biological activities, particularly in the context of medicinal chemistry. Compounds related to pyridine derivatives often exhibit a range of pharmacological effects, including:

  • Antimicrobial Activity: Some studies suggest that pyridine derivatives can inhibit bacterial growth.
  • Anti-inflammatory Properties: Certain derivatives have shown potential in reducing inflammation, making them candidates for anti-inflammatory drugs.
  • Analgesic Effects: Similar compounds have been linked to pain relief mechanisms.

The biological activity of 2,5-Pyridinediethanol may vary based on its specific structure and substituents.