structure of Pyridazine-4,5-diol

Pyridazine-4,5-diol

CAS No.: 55271-47-1
M. Wt: 112.08700
M. Fa: C4H4N2O2
InChI Key: PLYGYRGRWMDMDZ-UHFFFAOYSA-N

Names and Identifiers of Pyridazine-4,5-diol

CAS Number

55271-47-1

IUPAC Name

5-hydroxy-1H-pyridazin-4-one

InChI

InChI=1S/C4H4N2O2/c7-3-1-5-6-2-4(3)8/h1-2H,(H,5,8)(H,6,7)

InChIKey

PLYGYRGRWMDMDZ-UHFFFAOYSA-N

Canonical SMILES

C1=C(C(=O)C=NN1)O

Physical and chemical properties of Pyridazine-4,5-diol

Exact Mass

112.02700

Molecular Formula

C4H4N2O2

Molecular Weight

112.08700

PSA

66.24000

Storage condition

2-8°C

Applications of Pyridazine-4,5-diol

Pyridazine-4,5-diol finds applications across various fields:

  • Pharmaceuticals: Used as intermediates in the synthesis of drugs targeting bacterial infections and other diseases.
  • Agricultural Chemicals: Potential use in developing herbicides or fungicides due to its biological activity.
  • Material Science: Investigated for use in polymers and other materials owing to its unique chemical properties.

Interaction Studies of Pyridazine-4,5-diol

Studies have shown that pyridazine-4,5-diol interacts with several biomolecules:

  • Enzyme Interactions: It has been observed to inhibit certain enzymes linked to metabolic pathways, which may contribute to its pharmacological effects.
  • Protein Binding Studies: Research indicates that it can bind to specific proteins, altering their function and potentially leading to therapeutic effects.

Biological Activity of Pyridazine-4,5-diol

Pyridazine-4,5-diol exhibits notable biological activities. It has been found to interact with various enzymes and proteins, influencing biochemical pathways. Its derivatives have shown potential as:

  • Antimicrobial Agents: Some studies suggest that pyridazine derivatives possess antibacterial properties.
  • Antioxidants: The compound may act as an antioxidant due to its ability to donate electrons through the hydroxyl groups.
  • Pharmacological Agents: Research indicates potential applications in drug development, particularly in targeting specific biological pathways.