2-Bromophenylboronic acid
97%
- Product Code: 89817
Alias:
2-bromophenylboronic acid; 2-bromophenylboronic acid, 2-bromophenylboronic acid
CAS:
244205-40-1
| Molecular Weight: | 200.83 g./mol | Molecular Formula: | C₆H₆BBrO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01114672 | |
| Melting Point: | 113 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
2-Bromophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with diols and other functional groups. Its versatility and reactivity make it a crucial tool in modern synthetic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 109-114 |
| Purity | 97-100 |
| APPEARANCE | White to off-white solid |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿380.00 |
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| 5.000 | 10-20 days | ฿740.00 |
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| 25.000 | 10-20 days | ฿3,650.00 |
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| 100.000 | 10-20 days | ฿13,620.00 |
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2-Bromophenylboronic acid
2-Bromophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with diols and other functional groups. Its versatility and reactivity make it a crucial tool in modern synthetic chemistry.
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