3,5-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
97%
- Product Code: 178056
CAS:
1257641-28-3
| Molecular Weight: | 273.95 g./mol | Molecular Formula: | C₁₁H₁₄BCl₂NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12546037 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, inert gas |
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 with aryl or heteroaryl halides under palladium catalysis. It is especially valuable in medicinal chemistry for constructing complex pyridine-based scaffolds found in bioactive molecules. The presence of chlorine atoms offers additional sites for selective functionalization, enabling further structural diversification in drug discovery and materials science.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,070.00 |
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| 250mg | 10-20 days | ฿1,950.00 |
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| 1g | 10-20 days | ฿5,510.00 |
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3,5-Dichloro-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 with aryl or heteroaryl halides under palladium catalysis. It is especially valuable in medicinal chemistry for constructing complex pyridine-based scaffolds found in bioactive molecules. The presence of chlorine atoms offers additional sites for selective functionalization, enabling further structural diversification in drug discovery and materials science.
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