structure of 5-Methoxy-6-methyl-1H-indazole

5-Methoxy-6-methyl-1H-indazole

CAS No.: 1000343-61-2
M. Wt: 162.189
M. Fa: C9H10N2O
InChI Key: RGAHAJHHPKQPOG-UHFFFAOYSA-N

Names and Identifiers of 5-Methoxy-6-methyl-1H-indazole

CAS Number

1000343-61-2

IUPAC Name

5-methoxy-6-methyl-1H-indazole

InChI

InChI=1S/C9H10N2O/c1-6-3-8-7(5-10-11-8)4-9(6)12-2/h3-5H,1-2H3,(H,10,11)

InChIKey

RGAHAJHHPKQPOG-UHFFFAOYSA-N

Canonical SMILES

CC1=CC2=C(C=C1OC)C=NN2

Physical and chemical properties of 5-Methoxy-6-methyl-1H-indazole

Boiling Point

318.3±22.0 °C at 760 mmHg

Density

1.2±0.1 g/cm3

Exact Mass

162.079315

Flash Point

116.6±12.6 °C

Index of Refraction

1.629

LogP

2.19

Molecular Formula

C9H10N2O

Molecular Weight

162.189

PSA

37.91000

Storage condition

2-8°C

Vapour Pressure

0.0±0.7 mmHg at 25°C

Applications of 5-Methoxy-6-methyl-1H-indazole

5-Methoxy-6-methyl-1H-indazole has potential applications across various fields:

  • Medicinal Chemistry: Due to its biological activity, it is being explored for use in drug development targeting infectious diseases and cancer.
  • Material Science: Its unique chemical properties make it suitable for developing new materials with specific functionalities.

Current research is ongoing to explore its full potential in these areas.

Interaction Studies of 5-Methoxy-6-methyl-1H-indazole

Interaction studies involving 5-Methoxy-6-methyl-1H-indazole focus on understanding its binding affinity to various biological targets. Key areas of investigation include:

  • Enzyme Inhibition: Studies assess how this compound interacts with specific enzymes, which could lead to therapeutic applications.
  • Receptor Binding: Investigations into how 5-Methoxy-6-methyl-1H-indazole binds to receptors provide insights into its pharmacodynamics and potential side effects.

These studies are crucial for assessing safety and efficacy profiles necessary for clinical applications.

Biological Activity of 5-Methoxy-6-methyl-1H-indazole

Research indicates that 5-Methoxy-6-methyl-1H-indazole exhibits notable biological activities, including:

  • Antimicrobial Properties: Preliminary studies suggest that this compound may have antimicrobial effects against various pathogens.
  • Anticancer Activity: There is emerging evidence that 5-Methoxy-6-methyl-1H-indazole may inhibit cancer cell proliferation through various mechanisms, potentially making it a candidate for cancer therapy.
  • Neuroprotective Effects: Some studies have indicated potential neuroprotective properties, which could be beneficial in treating neurodegenerative diseases.

These activities highlight its relevance in pharmacological research and drug development.