4-Bromo-2-methylphenylboronic acid
95%
- Product Code: 90659
CAS:
221006-71-9
| Molecular Weight: | 214.9 g./mol | Molecular Formula: | C₇H₈BBrO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16660270 | |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
4-Bromo-2-methylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl halides or triflates in the presence of a palladium catalyst. Additionally, it serves as a building block in the development of bioactive compounds and functional polymers. Its stability and reactivity make it a valuable reagent in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿549.00 |
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| 1.000 | 10-20 days | ฿1,746.00 |
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4-Bromo-2-methylphenylboronic acid
4-Bromo-2-methylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, facilitating the coupling with aryl halides or triflates in the presence of a palladium catalyst. Additionally, it serves as a building block in the development of bioactive compounds and functional polymers. Its stability and reactivity make it a valuable reagent in medicinal chemistry for drug discovery and development.
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