1-(Tetrahydropyran-2-yl)-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-indazole
95%
- Product Code: 39751
CAS:
956388-05-9
| Molecular Weight: | 328.2137 g./mol | Molecular Formula: | C₁₈H₂₅BN₂O₃ |
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| EC Number: | MDL Number: | MFCD18207194 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate, particularly in the construction of complex molecules. Its tetrahydropyran and dioxaborolane groups make it valuable in cross-coupling reactions, such as Suzuki-Miyaura reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and advanced materials. The indazole core structure is often explored in drug discovery, as it is a common scaffold in biologically active compounds, including potential anticancer and anti-inflammatory agents. The boronate ester moiety enhances its reactivity and selectivity, making it a key component in the development of targeted therapies and functional materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £301.26 |
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1-(Tetrahydropyran-2-yl)-4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)-1H-indazole
This chemical is primarily utilized in organic synthesis as a versatile intermediate, particularly in the construction of complex molecules. Its tetrahydropyran and dioxaborolane groups make it valuable in cross-coupling reactions, such as Suzuki-Miyaura reactions, which are essential for forming carbon-carbon bonds in pharmaceuticals and advanced materials. The indazole core structure is often explored in drug discovery, as it is a common scaffold in biologically active compounds, including potential anticancer and anti-inflammatory agents. The boronate ester moiety enhances its reactivity and selectivity, making it a key component in the development of targeted therapies and functional materials.
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