2-Methoxy-4-methyl-3-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)pyridine
97%
- Product Code: 211374
CAS:
1420998-43-1
| Molecular Weight: | 249.11 g./mol | Molecular Formula: | C₁₃H₂₀BNO₃ |
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| EC Number: | MDL Number: | MFCD16995670 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs) and functional materials. The presence of the methoxy and methyl substituents enhances substrate selectivity and reaction yield in heterocyclic frameworks. Commonly employed in late-stage functionalization due to its stability and reactivity profile.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft24,904.60 |
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| 0.250 | 10-20 days | Ft59,897.14 |
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| 1.000 | 10-20 days | Ft207,328.19 |
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2-Methoxy-4-methyl-3-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)pyridine
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of active pharmaceutical ingredients (APIs) and functional materials. The presence of the methoxy and methyl substituents enhances substrate selectivity and reaction yield in heterocyclic frameworks. Commonly employed in late-stage functionalization due to its stability and reactivity profile.
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