2-(3-Fluoro-2-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
- Product Code: 41475
CAS:
1417301-67-7
| Molecular Weight: | 252.0896 g./mol | Molecular Formula: | C₁₃H₁₈BFO₃ |
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| EC Number: | MDL Number: | MFCD16996297 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a boron-containing reagent, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development and material science. The fluorine and methoxy substituents enhance its reactivity and selectivity in various catalytic processes. Additionally, it is employed in the preparation of advanced materials, such as organic semiconductors and polymers, due to its ability to introduce functional groups into molecular frameworks.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $23.76 |
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2-(3-Fluoro-2-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily used in organic synthesis as a boron-containing reagent, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronate ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development and material science. The fluorine and methoxy substituents enhance its reactivity and selectivity in various catalytic processes. Additionally, it is employed in the preparation of advanced materials, such as organic semiconductors and polymers, due to its ability to introduce functional groups into molecular frameworks.
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