1,6-Dimethyl-1H-pyrazolo[3,4-b]pyridine-4-carbaldehyde
97%
- Product Code: 39045
CAS:
1516833-31-0
| Molecular Weight: | 175.1873 g./mol | Molecular Formula: | C₉H₉N₃O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28955209 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis as a key intermediate for the development of various pharmaceuticals and biologically active compounds. Its structure is particularly valuable in the design and synthesis of novel drug candidates, especially those targeting neurological disorders and inflammatory diseases. Researchers leverage its pyrazolopyridine core to create molecules with potential therapeutic properties, such as kinase inhibitors or modulators of specific cellular pathways. Additionally, it serves as a building block in the preparation of complex heterocyclic compounds, which are often explored for their medicinal and agrochemical applications. Its aldehyde functional group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $207.92 |
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1,6-Dimethyl-1H-pyrazolo[3,4-b]pyridine-4-carbaldehyde
This chemical is primarily utilized in the field of organic synthesis as a key intermediate for the development of various pharmaceuticals and biologically active compounds. Its structure is particularly valuable in the design and synthesis of novel drug candidates, especially those targeting neurological disorders and inflammatory diseases. Researchers leverage its pyrazolopyridine core to create molecules with potential therapeutic properties, such as kinase inhibitors or modulators of specific cellular pathways. Additionally, it serves as a building block in the preparation of complex heterocyclic compounds, which are often explored for their medicinal and agrochemical applications. Its aldehyde functional group allows for further chemical modifications, enabling the creation of diverse derivatives with tailored properties.
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