2-(3,4-Dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 192943
CAS:
1467057-46-0
| Molecular Weight: | 276.14 g./mol | Molecular Formula: | C₁₅H₂₁BO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 376.2±31.0 °C(Predicted) | |
| Density: | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. It is especially useful when introducing the 3,4-dihydro-2H-benzo[b][1,4]dioxepin moiety, a scaffold found in bioactive molecules and drug candidates. The reagent enhances synthetic efficiency due to its stability and reactivity under mild conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 250mg | 10-20 days | $95.39 |
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| 1g | 10-20 days | $246.42 |
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| 5g | 10-20 days | $863.27 |
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2-(3,4-Dihydro-2H-benzo[b][1,4]dioxepin-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. It is especially useful when introducing the 3,4-dihydro-2H-benzo[b][1,4]dioxepin moiety, a scaffold found in bioactive molecules and drug candidates. The reagent enhances synthetic efficiency due to its stability and reactivity under mild conditions.
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