3-Bromo-7-chloro-1H-pyrazolo[3,4-c]pyridine
95%
- Product Code: 45329
CAS:
957760-22-4
| Molecular Weight: | 232.4700 g./mol | Molecular Formula: | C₆H₃BrClN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09265716 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for creating compounds with potential therapeutic applications. It is often employed in the design of drug candidates targeting central nervous system disorders, such as anxiety, depression, and neurodegenerative diseases. Additionally, it serves as a precursor in the development of kinase inhibitors, which are crucial in cancer therapy due to their role in regulating cell signaling pathways. Its reactivity allows for further functionalization, enabling researchers to explore a wide range of chemical modifications to optimize drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,331.00 |
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3-Bromo-7-chloro-1H-pyrazolo[3,4-c]pyridine
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both bromo and chloro substituents, makes it a versatile building block for creating compounds with potential therapeutic applications. It is often employed in the design of drug candidates targeting central nervous system disorders, such as anxiety, depression, and neurodegenerative diseases. Additionally, it serves as a precursor in the development of kinase inhibitors, which are crucial in cancer therapy due to their role in regulating cell signaling pathways. Its reactivity allows for further functionalization, enabling researchers to explore a wide range of chemical modifications to optimize drug efficacy and selectivity.
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