2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
96%
- Product Code: 41569
CAS:
1029439-49-3
| Molecular Weight: | 314.9863 g./mol | Molecular Formula: | C₁₃H₁₇BBrFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18434471 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for the formation of carbon-carbon bonds. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the bromomethyl group allows for further functionalization, enhancing its versatility in constructing diverse molecular frameworks. Additionally, its fluorophenyl moiety can contribute to the development of compounds with specific electronic properties, useful in materials science and drug design.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £94.25 |
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2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for the formation of carbon-carbon bonds. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the bromomethyl group allows for further functionalization, enhancing its versatility in constructing diverse molecular frameworks. Additionally, its fluorophenyl moiety can contribute to the development of compounds with specific electronic properties, useful in materials science and drug design.
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