1H-Pyrrolo[3,2-c]pyridine, 3-chloro-
Names and Identifiers of 1H-Pyrrolo[3,2-c]pyridine, 3-chloro-
CAS Number |
1000342-65-3 |
|---|---|
MDL Number |
MFCD08690127 |
IUPAC Name |
3-chloro-1H-pyrrolo[3,2-c]pyridine |
InChI |
InChI=1S/C7H5ClN2/c8-6-4-10-7-1-2-9-3-5(6)7/h1-4,10H |
InChIKey |
SMQIJLFZFORHTQ-UHFFFAOYSA-N |
Canonical SMILES |
ClC1=CNC2=CC=NC=C12 |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1H-Pyrrolo[3,2-c]pyridine, 3-chloro-
Boiling Point |
332.8±22.0 °C at 760 mmHg |
|---|---|
Density |
1.4±0.1 g/cm3 |
Exact Mass |
152.014130 |
Flash Point |
185.3±7.9 °C |
H Bond Acceptors |
1 |
H Bond Donors |
1 |
Index of Refraction |
1.703 |
LogP |
1.25 |
Molecular Formula |
C7H5ClN2 |
Molecular Weight |
152.581 |
PSA |
28.68000 |
Vapour Pressure |
0.0±0.7 mmHg at 25°C |
Safety Information of 1H-Pyrrolo[3,2-c]pyridine, 3-chloro-
Applications of 1H-Pyrrolo[3,2-c]pyridine, 3-chloro-
3-Chloro-1H-pyrrolo[3,2-c]pyridine finds applications in various fields:
- Pharmaceutical Development: Its derivatives are explored for their potential as therapeutic agents in cancer treatment and other diseases.
- Organic Synthesis: Acts as an intermediate in the synthesis of more complex organic molecules.
- Material Science: Potential use in developing new materials due to its unique electronic properties.
Interaction Studies of 1H-Pyrrolo[3,2-c]pyridine, 3-chloro-
Studies on the interactions of 3-chloro-1H-pyrrolo[3,2-c]pyridine with biological systems have revealed its ability to bind selectively to certain proteins and enzymes. This selectivity is crucial for its potential use in drug design, where targeting specific biological pathways can enhance therapeutic efficacy while minimizing side effects. Further research is ongoing to elucidate its mechanism of action at the molecular level.
Biological Activity of 1H-Pyrrolo[3,2-c]pyridine, 3-chloro-
Research indicates that 3-chloro-1H-pyrrolo[3,2-c]pyridine exhibits notable biological activities. It has been studied for its potential antiproliferative effects against various cancer cell lines, indicating its promise as an anticancer agent. Additionally, its derivatives have shown activity against melanoma cell lines, suggesting a role in targeted cancer therapies. The compound's unique structure allows it to interact with biological targets effectively.
