5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-3-carboxylic acid
96%
- Product Code: 244098
CAS:
1073354-94-5
| Molecular Weight: | 238.05 g./mol | Molecular Formula: | C₁₁H₁₅BO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09260445 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Drying, Inert Gas |
Product Description:
Used primarily in cross-coupling reactions, especially Suzuki-Miyaura coupling, to synthesize complex organic molecules. Its boronic ester functionality allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, enabling the formation of carbon-carbon bonds. This makes it valuable in pharmaceutical and agrochemical industries for building heteroaromatic frameworks. The furan ring provides a structural motif common in bioactive compounds, enhancing its utility in drug discovery and development. It is also employed in materials science for constructing conjugated systems in organic electronics.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,190.00 |
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| 1.000 | 10-20 days | ฿6,050.00 |
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| 5.000 | 10-20 days | ฿26,480.00 |
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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-3-carboxylic acid
Used primarily in cross-coupling reactions, especially Suzuki-Miyaura coupling, to synthesize complex organic molecules. Its boronic ester functionality allows it to react with aryl or vinyl halides in the presence of a palladium catalyst, enabling the formation of carbon-carbon bonds. This makes it valuable in pharmaceutical and agrochemical industries for building heteroaromatic frameworks. The furan ring provides a structural motif common in bioactive compounds, enhancing its utility in drug discovery and development. It is also employed in materials science for constructing conjugated systems in organic electronics.
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