6-Chloro-3H-imidazo[4,5-c]pyridin-4-amine
97%
- Product Code: 120534
CAS:
52559-17-8
| Molecular Weight: | 168.58 g./mol | Molecular Formula: | C₆H₅ClN₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18803412 | |
| Melting Point: | Boiling Point: | 561.1±45.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
6-Chloro-3H-imidazo[4,5-c]pyridin-4-amine is primarily utilized in pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzymes and receptors involved in disease pathways. Its structure is often exploited in the design of potential therapeutic agents, including kinase inhibitors, which are crucial in cancer treatment. Additionally, it is explored in the development of anti-inflammatory and antiviral drugs due to its ability to interact with specific molecular targets. Researchers also investigate its use in creating novel compounds for treating neurological disorders, leveraging its unique chemical framework to modulate brain-related processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $320.31 |
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| 0.250 | 10-20 days | $560.64 |
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| 1.000 | 10-20 days | $1,405.72 |
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6-Chloro-3H-imidazo[4,5-c]pyridin-4-amine
6-Chloro-3H-imidazo[4,5-c]pyridin-4-amine is primarily utilized in pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzymes and receptors involved in disease pathways. Its structure is often exploited in the design of potential therapeutic agents, including kinase inhibitors, which are crucial in cancer treatment. Additionally, it is explored in the development of anti-inflammatory and antiviral drugs due to its ability to interact with specific molecular targets. Researchers also investigate its use in creating novel compounds for treating neurological disorders, leveraging its unique chemical framework to modulate brain-related processes.
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