2-Methoxy-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
98%
- Product Code: 213333
CAS:
1083168-83-5
| Molecular Weight: | 249.11 g./mol | Molecular Formula: | C₁₃H₂₀BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12923400 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for constructing substituted pyridine derivatives, which are common scaffolds in drug discovery. The methoxy and methyl substituents help modulate electronic and steric properties, enhancing selectivity and yield in coupling reactions. Its stability and reactivity profile make it suitable for use in automated synthesis and library generation for high-throughput screening.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿4,230.00 |
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| 250mg | 10-20 days | ฿7,180.00 |
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| 5g | 10-20 days | ฿85,980.00 |
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| 1g | 10-20 days | ฿19,790.00 |
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2-Methoxy-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. It is especially useful for constructing substituted pyridine derivatives, which are common scaffolds in drug discovery. The methoxy and methyl substituents help modulate electronic and steric properties, enhancing selectivity and yield in coupling reactions. Its stability and reactivity profile make it suitable for use in automated synthesis and library generation for high-throughput screening.
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