1-(4-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethan-1-one
97%
- Product Code: 131120
CAS:
1688672-91-4
| Molecular Weight: | 276.14 g./mol | Molecular Formula: | C₁₅H₂₁BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24039878 | |
| Melting Point: | Boiling Point: | 406.1±35.0 °C(Predicted) | |
| Density: | 1.07±0.1 g/cm3(Predicted) | 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, agrochemical, and materials science research. It is especially useful for constructing substituted aromatic systems where a methoxy and acetyl group are retained in the final product. The compound’s stability and reactivity profile make it a preferred choice in late-stage functionalization during drug discovery and development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €39.30 |
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| 5.000 | 10-20 days | €145.78 |
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1-(4-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethan-1-one
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, agrochemical, and materials science research. It is especially useful for constructing substituted aromatic systems where a methoxy and acetyl group are retained in the final product. The compound’s stability and reactivity profile make it a preferred choice in late-stage functionalization during drug discovery and development.
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