Methyl 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
95%
- Product Code: 209449
CAS:
525362-07-6
| Molecular Weight: | 276.14 g./mol | Molecular Formula: | C₁₅H₂₁BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16996354 | |
| Melting Point: | Boiling Point: | 370.5±35.0 °C | |
| Density: | 1.07±0.1 g/cm3 | Storage Condition: | 2-8°C, dry |
Product Description:
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl systems. Its ester functionality allows further derivatization, such as hydrolysis to carboxylic acids or conversion to amides, enhancing its utility in drug discovery and materials science. Commonly employed in research laboratories for the preparation of intermediates in active pharmaceutical ingredients (APIs).
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | €39.00 |
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| 1g | 10-20 days | €91.18 |
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Methyl 2-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl systems. Its ester functionality allows further derivatization, such as hydrolysis to carboxylic acids or conversion to amides, enhancing its utility in drug discovery and materials science. Commonly employed in research laboratories for the preparation of intermediates in active pharmaceutical ingredients (APIs).
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