(3-Bromo-2,5-dimethylphenyl)boronic acid
97%
- Product Code: 117970
CAS:
1259318-83-6
| Molecular Weight: | 228.88 g./mol | Molecular Formula: | C₈H₁₀BBrO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12026703 | |
| Melting Point: | Boiling Point: | 363.3±52.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
(3-Bromo-2,5-dimethylphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate in cross-coupling reactions, such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including potential drug candidates. Its boronic acid group facilitates the formation of biaryl structures, which are common in many biologically active compounds. Additionally, it is used in material science for the development of organic electronic materials, where precise molecular architecture is crucial. The compound’s bromo and methyl substituents further enhance its reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿369.00 |
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| 0.250 | 10-20 days | ฿693.00 |
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(3-Bromo-2,5-dimethylphenyl)boronic acid
(3-Bromo-2,5-dimethylphenyl)boronic acid is primarily utilized in organic synthesis as a key intermediate in cross-coupling reactions, such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules, including potential drug candidates. Its boronic acid group facilitates the formation of biaryl structures, which are common in many biologically active compounds. Additionally, it is used in material science for the development of organic electronic materials, where precise molecular architecture is crucial. The compound’s bromo and methyl substituents further enhance its reactivity and selectivity in various chemical transformations.
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