2-(2-(Bromomethyl)-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
- Product Code: 43414
CAS:
850567-57-6
| Molecular Weight: | 314.9900 g./mol | Molecular Formula: | C₁₃H₁₇BBrFO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06659927 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the bromomethyl group allows for further functionalization, enhancing its utility in creating diverse chemical structures. Additionally, its fluorophenyl moiety can contribute to the development of compounds with specific biological activities, often exploited in drug discovery and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,032.00 |
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2-(2-(Bromomethyl)-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the bromomethyl group allows for further functionalization, enhancing its utility in creating diverse chemical structures. Additionally, its fluorophenyl moiety can contribute to the development of compounds with specific biological activities, often exploited in drug discovery and material science.
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