3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
- Product Code: 210002
CAS:
1032358-00-1
| Molecular Weight: | 219.09 g./mol | Molecular Formula: | C₁₂H₁₈BNO₂ |
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| EC Number: | MDL Number: | MFCD07374972 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in medicinal chemistry for constructing substituted pyridine derivatives, which are common motifs in bioactive molecules. The presence of the methyl group enhances reactivity and selectivity in coupling processes, making it useful in the development of complex organic structures for drug discovery and materials science.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,120.00 |
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| 250mg | 10-20 days | ฿3,530.00 |
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| 1g | 10-20 days | ฿11,080.00 |
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| 5g | 10-20 days | ฿48,040.00 |
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3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in medicinal chemistry for constructing substituted pyridine derivatives, which are common motifs in bioactive molecules. The presence of the methyl group enhances reactivity and selectivity in coupling processes, making it useful in the development of complex organic structures for drug discovery and materials science.
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