3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indazole
97%
- Product Code: 171330
CAS:
1421252-90-5
| Molecular Weight: | 426.34 g./mol | Molecular Formula: | C₂₂H₂₇BN₂O₄S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 594.3±60.0°C | |
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in constructing complex indazole-based scaffolds found in bioactive molecules and drug candidates. Commonly applied in the development of kinase inhibitors and other therapeutic agents where precise molecular architecture is critical. Stable and compatible with a range of functional groups, it supports efficient and selective late-stage functionalization in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 25mg | 10-20 days | ฿4,160.00 |
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| 100mg | 10-20 days | ฿9,790.00 |
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3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-tosyl-1H-indazole
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its boronate ester group facilitates coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in constructing complex indazole-based scaffolds found in bioactive molecules and drug candidates. Commonly applied in the development of kinase inhibitors and other therapeutic agents where precise molecular architecture is critical. Stable and compatible with a range of functional groups, it supports efficient and selective late-stage functionalization in medicinal chemistry research.
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