4,4,5,5-Tetramethyl-2-(2-phenylpropyl)-1,3,2-dioxaborolane
98%
- Product Code: 243495
CAS:
280559-30-0
| Molecular Weight: | 246.16 g./mol | Molecular Formula: | C₁₅H₂₃BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953475 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Inert Gas |
Product Description:
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable boronic ester equivalent, enabling the formation of carbon-carbon bonds between aromatic or alkenyl halides and boron-containing partners. Its steric bulk and electron-donating groups enhance stability and selectivity, making it valuable in pharmaceutical and agrochemical synthesis where precise molecular construction is critical. Commonly employed in late-stage functionalization due to its tolerance of various functional groups and mild reaction conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft23,439.04 |
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| 1.000 | 10-20 days | Ft70,422.22 |
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| 5.000 | 10-20 days | Ft351,690.67 |
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| 0.100 | 10-20 days | Ft14,609.98 |
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4,4,5,5-Tetramethyl-2-(2-phenylpropyl)-1,3,2-dioxaborolane
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable boronic ester equivalent, enabling the formation of carbon-carbon bonds between aromatic or alkenyl halides and boron-containing partners. Its steric bulk and electron-donating groups enhance stability and selectivity, making it valuable in pharmaceutical and agrochemical synthesis where precise molecular construction is critical. Commonly employed in late-stage functionalization due to its tolerance of various functional groups and mild reaction conditions.
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