(5-Fluoro-1-methyl-1H-indazol-6-yl)boronic acid
97%
- Product Code: 192576
CAS:
2096331-06-3
| Molecular Weight: | 193.97 g./mol | Molecular Formula: | C₈H₈BFN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18089818 | |
| Melting Point: | Boiling Point: | 397.7±52.0 °C(Predicted) | |
| Density: | 1.37±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of complex organic molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the indazole core’s ability to mimic purine bases, enhancing binding affinity to biological targets. Also utilized in the preparation of fluorescent probes and bioactive molecule labeling through boronate-based conjugation strategies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿4,080.00 |
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| 0.250 G | 10-20 days | ฿6,990.00 |
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(5-Fluoro-1-methyl-1H-indazol-6-yl)boronic acid
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing efficient construction of complex organic molecules. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the indazole core’s ability to mimic purine bases, enhancing binding affinity to biological targets. Also utilized in the preparation of fluorescent probes and bioactive molecule labeling through boronate-based conjugation strategies.
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