(4,5-Difluoro-2-methylphenyl)boronic acid
97%
- Product Code: 87093
CAS:
1416244-48-8
| Molecular Weight: | 171.94 g./mol | Molecular Formula: | C₇H₇BF₂O₂ |
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| EC Number: | MDL Number: | MFCD12911676 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
(4,5-Difluoro-2-methylphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create complex biaryl compounds, which are essential intermediates in the production of various drugs. The compound’s boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse organic molecules.
Additionally, it finds application in material science, where it is used to develop advanced polymers and organic electronic materials. Its ability to act as a building block in the creation of functionalized aromatic compounds makes it valuable in designing materials with specific properties, such as improved conductivity or stability.
In research, it serves as a reagent for studying reaction mechanisms and developing new synthetic methodologies. Its unique structure, with fluorine and methyl substituents, allows for fine-tuning reactivity and selectivity in chemical transformations, making it a versatile tool in both academic and industrial laboratories.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,269.00 |
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| 1.000 | 10-20 days | ฿3,564.00 |
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| 5.000 | 10-20 days | ฿12,798.00 |
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(4,5-Difluoro-2-methylphenyl)boronic acid
(4,5-Difluoro-2-methylphenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create complex biaryl compounds, which are essential intermediates in the production of various drugs. The compound’s boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse organic molecules.
Additionally, it finds application in material science, where it is used to develop advanced polymers and organic electronic materials. Its ability to act as a building block in the creation of functionalized aromatic compounds makes it valuable in designing materials with specific properties, such as improved conductivity or stability.
In research, it serves as a reagent for studying reaction mechanisms and developing new synthetic methodologies. Its unique structure, with fluorine and methyl substituents, allows for fine-tuning reactivity and selectivity in chemical transformations, making it a versatile tool in both academic and industrial laboratories.
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