2-(Bromomethyl)phenylboronic acid
98%
- Product Code: 89701
CAS:
91983-14-1
| Molecular Weight: | 214.85 g./mol | Molecular Formula: | C₇H₈BBrO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318941 | |
| Melting Point: | 145-148 | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the bromomethyl group offers further functionalization opportunities, allowing for the introduction of diverse substituents or linkages in target molecules. Its applications extend to the development of bioactive compounds and polymers, where precise molecular architecture is essential.
Product Specification:
| Test | Specification |
|---|---|
| PURITYTITRATION WITH AGNO3 | 98-100 |
| APPEARANCE | White to tan powder or crystals |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿450.00 |
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| 1.000 | 10-20 days | ฿1,140.00 |
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| 5.000 | 10-20 days | ฿3,350.00 |
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| 25.000 | 10-20 days | ฿15,680.00 |
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2-(Bromomethyl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the bromomethyl group offers further functionalization opportunities, allowing for the introduction of diverse substituents or linkages in target molecules. Its applications extend to the development of bioactive compounds and polymers, where precise molecular architecture is essential.
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