2-(2-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
- Product Code: 115616
CAS:
1192548-08-5
| Molecular Weight: | 236.09 g./mol | Molecular Formula: | C₁₃H₁₈BFO₂ |
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| EC Number: | MDL Number: | MFCD18384075 | |
| Melting Point: | Boiling Point: | 308.5±35.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. Its application is significant in pharmaceutical research and development, where it aids in the synthesis of drug candidates and bioactive compounds. Additionally, it is utilized in material science for creating advanced polymers and functional materials. The fluorine and methyl groups on the phenyl ring enhance its reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $11.88 |
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| 1.000 | 10-20 days | $26.73 |
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| 5.000 | 10-20 days | $107.20 |
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2-(2-Fluoro-3-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. Its application is significant in pharmaceutical research and development, where it aids in the synthesis of drug candidates and bioactive compounds. Additionally, it is utilized in material science for creating advanced polymers and functional materials. The fluorine and methyl groups on the phenyl ring enhance its reactivity and selectivity in various chemical transformations.
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