3-Bromo-4-chloro-1H-pyrazolo[3,4-b]pyridine
97%
- Product Code: 65117
CAS:
1357945-38-0
| Molecular Weight: | 232.47 g./mol | Molecular Formula: | C₆H₃BrClN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22380452 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents, especially those targeting kinase inhibition. Researchers often employ it to create novel compounds with potential therapeutic applications, such as anti-cancer, anti-inflammatory, or anti-viral drugs. Additionally, its unique pyrazolo[3,4-b]pyridine core makes it a versatile building block in organic synthesis, enabling the exploration of new chemical spaces for drug discovery. Its halogenated nature also allows for further functionalization, enhancing its utility in designing complex molecules with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,064.00 |
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| 0.250 | 10-20 days | ฿13,698.00 |
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| 1.000 | 10-20 days | ฿36,972.00 |
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3-Bromo-4-chloro-1H-pyrazolo[3,4-b]pyridine
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents, especially those targeting kinase inhibition. Researchers often employ it to create novel compounds with potential therapeutic applications, such as anti-cancer, anti-inflammatory, or anti-viral drugs. Additionally, its unique pyrazolo[3,4-b]pyridine core makes it a versatile building block in organic synthesis, enabling the exploration of new chemical spaces for drug discovery. Its halogenated nature also allows for further functionalization, enhancing its utility in designing complex molecules with specific biological activities.
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