6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile
95%
- Product Code: 81499
CAS:
1073353-83-9
| Molecular Weight: | 230.07 g./mol | Molecular Formula: | C₁₂H₁₅BN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07367521 | |
| Melting Point: | Boiling Point: | 358 °C | |
| Density: | 1.10 g/cm3 | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. Its boronate ester group facilitates efficient coupling with aryl halides, making it valuable in pharmaceutical research for constructing drug candidates. Additionally, it serves as a building block in the development of agrochemicals and functional materials, particularly in the synthesis of heterocyclic compounds. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for creating diverse chemical libraries.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿12,600.00 |
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| 0.025 | 10-20 days | ฿26,980.00 |
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| 0.100 | 10-20 days | ฿64,800.00 |
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile
Widely used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex molecules. Its boronate ester group facilitates efficient coupling with aryl halides, making it valuable in pharmaceutical research for constructing drug candidates. Additionally, it serves as a building block in the development of agrochemicals and functional materials, particularly in the synthesis of heterocyclic compounds. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for creating diverse chemical libraries.
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