structure of 4-fluoro-7-methoxy-1H-indazole

4-fluoro-7-methoxy-1H-indazole

CAS No.: 1000341-74-1
M. Wt: 166.152
M. Fa: C8H7FN2O
InChI Key: IMRWTEVYVSFJKW-UHFFFAOYSA-N

Names and Identifiers of 4-fluoro-7-methoxy-1H-indazole

CAS Number

1000341-74-1

IUPAC Name

4-fluoro-7-methoxy-1H-indazole

InChI

InChI=1S/C8H7FN2O/c1-12-7-3-2-6(9)5-4-10-11-8(5)7/h2-4H,1H3,(H,10,11)

InChIKey

IMRWTEVYVSFJKW-UHFFFAOYSA-N

Canonical SMILES

COC1=C2C(=C(C=C1)F)C=NN2

Physical and chemical properties of 4-fluoro-7-methoxy-1H-indazole

Boiling Point

330.5±22.0 °C at 760 mmHg

Density

1.3±0.1 g/cm3

Exact Mass

166.054245

Flash Point

153.7±22.3 °C

Index of Refraction

1.620

LogP

1.86

Molecular Formula

C8H7FN2O

Molecular Weight

166.152

PSA

37.91000

Vapour Pressure

0.0±0.7 mmHg at 25°C

Safety Information of 4-fluoro-7-methoxy-1H-indazole

Pictograms

Signal Word

 Warning

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

Applications of 4-fluoro-7-methoxy-1H-indazole

4-fluoro-7-methoxy-1H-indazole has several applications in various fields:

  • Medicinal Chemistry: It serves as a building block for synthesizing more complex drug candidates with potential therapeutic effects.
  • Biological Research: The compound is studied for its role in understanding biological mechanisms and pathways due to its unique chemical structure.
  • Chemical Manufacturing: It is utilized as an intermediate in developing new materials and compounds in industrial processes.

Interaction Studies of 4-fluoro-7-methoxy-1H-indazole

Research into the interaction mechanisms of 4-fluoro-7-methoxy-1H-indazole suggests that it may act on specific molecular targets such as protein kinases or other enzymes involved in disease pathways. The unique arrangement of fluorine and methoxy groups enhances its selectivity and binding affinity, making it a valuable compound for further studies in drug design and development.

Biological Activity of 4-fluoro-7-methoxy-1H-indazole

4-fluoro-7-methoxy-1H-indazole exhibits significant biological activity, making it a subject of interest in pharmacological research. It has been investigated for its potential antimicrobial, anticancer, and anti-inflammatory properties. The presence of fluorine and methoxy groups enhances its binding affinity to specific enzymes or receptors, potentially leading to inhibition or modulation of various biological pathways.