3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
98%
- Product Code: 204167
CAS:
864771-17-5
| Molecular Weight: | 258.12 g./mol | Molecular Formula: | C₁₄H₁₉BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07779192 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or heteroaryl frameworks found in pharmaceuticals and agrochemicals. The indazole core is a common motif in bioactive molecules, making this compound valuable in drug discovery for developing kinase inhibitors and other therapeutic agents. Its boronate ester group offers good stability and reactivity under palladium catalysis, allowing efficient derivatization of the indazole scaffold under mild conditions. Frequently employed in medicinal chemistry research for library synthesis and structure-activity relationship studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,370.00 |
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| 250mg | 10-20 days | ฿3,730.00 |
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3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or heteroaryl frameworks found in pharmaceuticals and agrochemicals. The indazole core is a common motif in bioactive molecules, making this compound valuable in drug discovery for developing kinase inhibitors and other therapeutic agents. Its boronate ester group offers good stability and reactivity under palladium catalysis, allowing efficient derivatization of the indazole scaffold under mild conditions. Frequently employed in medicinal chemistry research for library synthesis and structure-activity relationship studies.
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