Methyl 5-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)pyrimidine-2-carboxylate
98%
- Product Code: 211393
CAS:
1610705-51-5
| Molecular Weight: | 264.09 g./mol | Molecular Formula: | C₁₂H₁₇BN₂O₄ |
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| EC Number: | MDL Number: | MFCD16618882 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The pyrimidine ring enhances binding affinity in bioactive compounds, allowing its use in constructing nitrogen-containing heterocycles for medicinal chemistry applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿1,560.00 |
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| 250mg | 10-20 days | ฿2,250.00 |
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| 1g | 10-20 days | ฿5,510.00 |
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| 5g | 10-20 days | ฿27,410.00 |
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Methyl 5-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)pyrimidine-2-carboxylate
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The pyrimidine ring enhances binding affinity in bioactive compounds, allowing its use in constructing nitrogen-containing heterocycles for medicinal chemistry applications.
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