2-(2-Methoxyethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
98%
- Product Code: 211833
CAS:
1257553-79-9
| Molecular Weight: | 279.15 g./mol | Molecular Formula: | C₁₄H₂₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16995934 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of carbon-carbon bonds under mild conditions. It is especially valuable in the preparation of complex pyridine-containing molecules, which are common structural motifs in bioactive compounds. The methoxyethoxy substituent enhances solubility and stability, improving reaction yields in aqueous or mixed solvent systems. Widely applied in medicinal chemistry for lead optimization and in materials science for constructing functional organic frameworks.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,360.00 |
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| 5g | 10-20 days | ฿15,480.00 |
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| 1g | 10-20 days | ฿3,560.00 |
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2-(2-Methoxyethoxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of carbon-carbon bonds under mild conditions. It is especially valuable in the preparation of complex pyridine-containing molecules, which are common structural motifs in bioactive compounds. The methoxyethoxy substituent enhances solubility and stability, improving reaction yields in aqueous or mixed solvent systems. Widely applied in medicinal chemistry for lead optimization and in materials science for constructing functional organic frameworks.
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