N-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
98%
- Product Code: 116954
CAS:
1005009-98-2
| Molecular Weight: | 234.1 g./mol | Molecular Formula: | C₁₂H₁₉BN₂O₂ |
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| EC Number: | MDL Number: | MFCD11878220 | |
| Melting Point: | Boiling Point: | 352.7±27.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds and materials for electronic applications due to its stability and reactivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $110.74 |
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| 0.250 | 10-20 days | $167.38 |
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| 1.000 | 10-20 days | $361.39 |
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N-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable for creating carbon-carbon bonds. Additionally, it is employed in the synthesis of bioactive compounds and materials for electronic applications due to its stability and reactivity.
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