N-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxamide
95%
- Product Code: 218176
CAS:
1313738-91-8
| Molecular Weight: | 262.11 g./mol | Molecular Formula: | C₁₃H₁₉BN₂O₃ |
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| EC Number: | MDL Number: | MFCD11878164 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex pyridine-containing molecules for drug discovery. The N-methylcarboxamide moiety enhances stability and influences electronic properties, improving reaction selectivity and yield in medicinal chemistry applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 1g | 10-20 days | $74.79 |
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| 5g | 10-20 days | $332.07 |
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N-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-carboxamide
Used in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates efficient coupling with aryl halides under palladium catalysis, making it valuable in the preparation of complex pyridine-containing molecules for drug discovery. The N-methylcarboxamide moiety enhances stability and influences electronic properties, improving reaction selectivity and yield in medicinal chemistry applications.
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