1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
97%
- Product Code: 208726
CAS:
1256359-09-7
| Molecular Weight: | 258.12 g./mol | Molecular Formula: | C₁₄H₁₉BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15071439 | |
| Melting Point: | Boiling Point: | 385.0±15.0°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, stored in inert gas |
Product Description:
Used primarily as a key intermediate in pharmaceutical synthesis, especially in the development of kinase inhibitors and other biologically active compounds. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in drug discovery programs. Commonly employed in the preparation of potential anticancer, anti-inflammatory, and antiviral agents due to its indazole core, which is known for favorable binding to various enzyme targets. Also utilized in research settings for the rapid assembly of complex molecules through palladium-catalyzed transformations.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿860.00 |
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| 250mg | 10-20 days | ฿1,450.00 |
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| 1g | 10-20 days | ฿2,620.00 |
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1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
Used primarily as a key intermediate in pharmaceutical synthesis, especially in the development of kinase inhibitors and other biologically active compounds. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in drug discovery programs. Commonly employed in the preparation of potential anticancer, anti-inflammatory, and antiviral agents due to its indazole core, which is known for favorable binding to various enzyme targets. Also utilized in research settings for the rapid assembly of complex molecules through palladium-catalyzed transformations.
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