2-(2,3-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
- Product Code: 178047
CAS:
1232132-73-8
| Molecular Weight: | 232.13 g./mol | Molecular Formula: | C₁₄H₂₁BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18383605 | |
| Melting Point: | Boiling Point: | 330.2±31.0 °C(Predicted) | |
| Density: | 0.97±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, dry |
Product Description:
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure makes it valuable for constructing biaryl compounds, which are common in pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a stable, easily handled boronic ester equivalent, offering improved selectivity and yield in coupling processes. It is particularly useful in the development of complex aromatic systems where precise substitution patterns are required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿720.00 |
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| 1g | 10-20 days | ฿1,900.00 |
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| 5g | 10-20 days | ฿6,840.00 |
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2-(2,3-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its boron-containing structure makes it valuable for constructing biaryl compounds, which are common in pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a stable, easily handled boronic ester equivalent, offering improved selectivity and yield in coupling processes. It is particularly useful in the development of complex aromatic systems where precise substitution patterns are required.
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