3-Bromo-5-fluorobenzeneboronic acid
98%
- Product Code: 89154
CAS:
849062-37-9
Molecular Weight: | 218.82 g./mol | Molecular Formula: | C₆H₅BBrFO₂ |
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EC Number: | MDL Number: | MFCD06411356 | |
Melting Point: | >300°C | Boiling Point: | |
Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely utilized in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, enabling the construction of complex biaryl structures. Such structures are fundamental in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its bromo and fluoro substituents enhance its reactivity and selectivity in these coupling reactions, making it a valuable intermediate in the synthesis of diverse organic compounds. Its application extends to the preparation of bioactive molecules and polymers, where precise molecular architecture is crucial.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿612.00 |
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5.000 | 10-20 days | ฿2,340.00 |
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25.000 | 10-20 days | ฿8,757.00 |
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3-Bromo-5-fluorobenzeneboronic acid
This compound is widely utilized in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, enabling the construction of complex biaryl structures. Such structures are fundamental in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its bromo and fluoro substituents enhance its reactivity and selectivity in these coupling reactions, making it a valuable intermediate in the synthesis of diverse organic compounds. Its application extends to the preparation of bioactive molecules and polymers, where precise molecular architecture is crucial.
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