3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
95%
- Product Code: 242533
CAS:
1073354-97-8
| Molecular Weight: | 220.07 g./mol | Molecular Formula: | C₁₁H₁₇BN₂O₂ |
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| EC Number: | MDL Number: | MFCD09260488 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inflatable, avoiding light |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in drug discovery and development, especially for constructing complex nitrogen-containing heterocyclic systems. It is also employed in materials science for designing organic electronic materials due to its stable and reactive boronate ester functionality.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿3,200.00 |
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| 5g | 10-20 days | ฿13,090.00 |
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| 10g | 10-20 days | ฿24,550.00 |
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| 25g | 10-20 days | ฿58,930.00 |
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in drug discovery and development, especially for constructing complex nitrogen-containing heterocyclic systems. It is also employed in materials science for designing organic electronic materials due to its stable and reactive boronate ester functionality.
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