5-Fluoro-3-iodo-1H-pyrazolo[3,4-b]pyridine
98%
- Product Code: 119890
CAS:
1350653-23-4
| Molecular Weight: | 263.01 g./mol | Molecular Formula: | C₆H₃FIN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20923264 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Primarily utilized in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for treating cancers and inflammatory diseases. Researchers leverage its unique chemical framework to design and optimize drug candidates that target specific enzymes involved in disease pathways. Additionally, it is explored in the creation of novel therapeutic compounds aimed at addressing neurological disorders, owing to its ability to interact with biological targets in the central nervous system. Its halogenated pyrazolopyridine core also makes it a promising candidate for further chemical modifications, enabling the discovery of new bioactive molecules.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,035.00 |
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| 0.250 | 10-20 days | ฿2,052.00 |
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| 1.000 | 10-20 days | ฿5,517.00 |
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| 5.000 | 10-20 days | ฿19,287.00 |
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5-Fluoro-3-iodo-1H-pyrazolo[3,4-b]pyridine
Primarily utilized in the field of medicinal chemistry, this compound serves as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of kinase inhibitors, which are crucial for treating cancers and inflammatory diseases. Researchers leverage its unique chemical framework to design and optimize drug candidates that target specific enzymes involved in disease pathways. Additionally, it is explored in the creation of novel therapeutic compounds aimed at addressing neurological disorders, owing to its ability to interact with biological targets in the central nervous system. Its halogenated pyrazolopyridine core also makes it a promising candidate for further chemical modifications, enabling the discovery of new bioactive molecules.
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