Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinate
95%
- Product Code: 210213
CAS:
957062-72-5
| Molecular Weight: | 263.10 g./mol | Molecular Formula: | C₁₃H₁₈BNO₄ |
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| EC Number: | MDL Number: | MFCD08752647 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inert gas storage |
Product Description:
Used primarily in cross-coupling reactions such as Suzuki-Miyaura coupling, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, making it valuable in medicinal chemistry for constructing biaryl systems. It is especially useful in the development of drug candidates where a pyridine moiety is required, due to the presence of the methyl picolinate group. The compound’s stability and reactivity profile allow for high yields under mild conditions, which is advantageous in both research and industrial settings.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | $42.30 |
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| 250mg | 10-20 days | $64.65 |
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| 1g | 10-20 days | $204.32 |
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| 5g | 10-20 days | $766.21 |
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| 25g | 10-20 days | $2,873.30 |
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Methyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinate
Used primarily in cross-coupling reactions such as Suzuki-Miyaura coupling, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation with aryl or heteroaryl halides, making it valuable in medicinal chemistry for constructing biaryl systems. It is especially useful in the development of drug candidates where a pyridine moiety is required, due to the presence of the methyl picolinate group. The compound’s stability and reactivity profile allow for high yields under mild conditions, which is advantageous in both research and industrial settings.
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