3-Cyclopropyl-6-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)-1H-indazole
98%
- Product Code: 164093
CAS:
1650548-68-7
| Molecular Weight: | 284.16 g./mol | Molecular Formula: | C₁₆H₂₁BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27936578 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to develop biologically active compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the preparation of indazole-based drug candidates. Commonly applied in research for developing kinase inhibitors and oncology-related therapeutics. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the indazole core’s ability to mimic purine bases in biological systems.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,950.00 |
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| 1g | 10-20 days | ฿8,950.00 |
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| 250mg | 10-20 days | ฿3,320.00 |
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3-Cyclopropyl-6-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)-1H-indazole
Used as a key intermediate in pharmaceutical synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to develop biologically active compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the preparation of indazole-based drug candidates. Commonly applied in research for developing kinase inhibitors and oncology-related therapeutics. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the indazole core’s ability to mimic purine bases in biological systems.
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