2-(2-Bromo-5-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
≥95%
- Product Code: 140769
CAS:
1256781-63-1
| Molecular Weight: | 317.41 g./mol | Molecular Formula: | C₁₂H₁₅BO₂ClBr |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17215818 | |
| Melting Point: | Boiling Point: | 362.1±32.0 °C(Predicted) | |
| Density: | 1.38±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, inert gas |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical, agrochemical, and materials science research. The presence of bromo and chloro substituents allows for selective, stepwise coupling reactions, offering precise control in multi-step syntheses. It is especially useful in constructing biaryl systems found in bioactive compounds and functional materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €189.50 |
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| 1.000 | 10-20 days | €786.37 |
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| 5.000 | 10-20 days | €2,750.59 |
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2-(2-Bromo-5-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical, agrochemical, and materials science research. The presence of bromo and chloro substituents allows for selective, stepwise coupling reactions, offering precise control in multi-step syntheses. It is especially useful in constructing biaryl systems found in bioactive compounds and functional materials.
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