4-chloro-7-fluoro-1H-indole
CAS No.:
1000341-78-5
M. Wt:
169.583
M. Fa:
C8H5ClFN
InChI Key:
KWILNHHBZCXENW-UHFFFAOYSA-N
Names and Identifiers of 4-chloro-7-fluoro-1H-indole
CAS Number |
1000341-78-5 |
|---|---|
EC Number |
867-141-5 |
MDL Number |
MFCD03095315 |
IUPAC Name |
4-chloro-7-fluoro-1H-indole |
InChI |
InChI=1S/C8H5ClFN/c9-6-1-2-7(10)8-5(6)3-4-11-8/h1-4,11H |
InChIKey |
KWILNHHBZCXENW-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC(=C2C=CNC2=C1F)Cl |
UNSPSC Code |
12352100 |
Physical and chemical properties of 4-chloro-7-fluoro-1H-indole
Boiling Point |
295.4±20.0 °C at 760 mmHg |
|---|---|
Density |
1.4±0.1 g/cm3 |
Exact Mass |
169.009460 |
Flash Point |
132.5±21.8 °C |
H Bond Acceptors |
0 |
H Bond Donors |
1 |
Index of Refraction |
1.657 |
LogP |
2.74 |
Molecular Formula |
C8H5ClFN |
Molecular Weight |
169.583 |
PSA |
15.79000 |
Vapour Pressure |
0.0±0.6 mmHg at 25°C |
Safety Information of 4-chloro-7-fluoro-1H-indole
Applications of 4-chloro-7-fluoro-1H-indole
4-Chloro-7-fluoro-1H-indole has several applications, particularly in:
- Medicinal Chemistry: As a lead compound for developing new therapeutic agents targeting various diseases.
- Biochemical Research: Utilized in studies involving enzyme inhibition and protein interaction assays.
- Material Science: Potential use in organic electronics and photonic devices due to its unique electronic properties.
Interaction Studies of 4-chloro-7-fluoro-1H-indole
Studies on the interactions of 4-chloro-7-fluoro-1H-indole with biological macromolecules reveal its potential as a modulator of enzyme activity and cellular signaling pathways. The compound can induce conformational changes in target proteins, altering their function and potentially leading to therapeutic outcomes.
Biological Activity of 4-chloro-7-fluoro-1H-indole
Indole derivatives, including 4-chloro-7-fluoro-1H-indole, exhibit a wide range of biological activities. These include:
- Antiviral: Potential effectiveness against various viral infections.
- Anti-inflammatory: Ability to reduce inflammation in biological tissues.
- Anticancer: Inhibition of cancer cell proliferation through various mechanisms.
- Antimicrobial: Activity against bacteria and fungi.
The compound's interactions with enzymes and proteins can lead to significant changes in cellular processes, influencing pathways related to cell proliferation, differentiation, and apoptosis.
