(3-Bromo-2-methylphenyl)boronic acid
95%
- Product Code: 36683
CAS:
1184298-27-8
Molecular Weight: | 214.85 g./mol | Molecular Formula: | C₇H₈BBrO₂ |
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EC Number: | MDL Number: | MFCD18447597 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20℃, inert gas |
Product Description:
(3-Bromo-2-methylphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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, enabling the introduction of the (3-bromo-2-methylphenyl) group into target structures. Its boronic acid functionality allows for efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is used in the development of bioactive compounds and in research focused on creating novel chemical entities for drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿2,700.00 |
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1.000 | 10-20 days | ฿10,242.00 |
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5.000 | 10-20 days | ฿32,040.00 |
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(3-Bromo-2-methylphenyl)boronic acid
(3-Bromo-2-methylphenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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, enabling the introduction of the (3-bromo-2-methylphenyl) group into target structures. Its boronic acid functionality allows for efficient coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it is used in the development of bioactive compounds and in research focused on creating novel chemical entities for drug discovery.
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