(2,5-Dibromopyridin-4-yl)boronic acid
98%
- Product Code: 88986
CAS:
1031843-77-2
Molecular Weight: | 280.72 g./mol | Molecular Formula: | C₅H₄BBr₂NO₂ |
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EC Number: | MDL Number: | MFCD11109338 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
(2,5-Dibromopyridin-4-yl)boronic acid is primarily used in organic synthesis as a versatile building block for the creation of complex molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The dibromo substitution on the pyridine ring further enhances its reactivity, allowing for selective functionalization and the construction of diverse heterocyclic compounds. Additionally, it is utilized in the development of sensors and ligands due to its ability to interact with various metal ions and organic substrates.
Product Specification:
Test | Specification |
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PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.500 | 10-20 days | ฿4,000.00 |
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1.000 | 10-20 days | ฿5,810.00 |
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(2,5-Dibromopyridin-4-yl)boronic acid
(2,5-Dibromopyridin-4-yl)boronic acid is primarily used in organic synthesis as a versatile building block for the creation of complex molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The dibromo substitution on the pyridine ring further enhances its reactivity, allowing for selective functionalization and the construction of diverse heterocyclic compounds. Additionally, it is utilized in the development of sensors and ligands due to its ability to interact with various metal ions and organic substrates.
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