2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
≥95%
- Product Code: 193955
CAS:
1189746-27-7
| Molecular Weight: | 258.12 g./mol | Molecular Formula: | C₁₄H₁₉BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11109436 | |
| Melting Point: | Boiling Point: | 404.4±18.0 °C(Predicted) | |
| Density: | 1.11±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing complex indazole-based structures, which are common in bioactive molecules and drug candidates. Due to its stability and reactivity, it is widely employed in medicinal chemistry for lead optimization and library synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,520.00 |
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| 250mg | 10-20 days | ฿2,480.00 |
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| 1g | 10-20 days | ฿7,100.00 |
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| 5g | 10-20 days | ฿21,880.00 |
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| 10g | 10-20 days | ฿43,730.00 |
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2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing complex indazole-based structures, which are common in bioactive molecules and drug candidates. Due to its stability and reactivity, it is widely employed in medicinal chemistry for lead optimization and library synthesis.
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