2-(2-Fluoro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
- Product Code: 62292
CAS:
1599432-41-3
| Molecular Weight: | 252.09 g./mol | Molecular Formula: | C₁₃H₁₈BFO₃ |
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| EC Number: | MDL Number: | MFCD16996294 | |
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| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in constructing complex organic molecules. Additionally, it is employed in the synthesis of heterocyclic compounds and as an intermediate in the production of bioactive molecules, contributing to drug discovery and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,359.00 |
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| 1.000 | 10-20 days | ฿3,384.00 |
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| 5.000 | 10-20 days | ฿13,527.00 |
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2-(2-Fluoro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in constructing complex organic molecules. Additionally, it is employed in the synthesis of heterocyclic compounds and as an intermediate in the production of bioactive molecules, contributing to drug discovery and material science research.
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