3-(Acetyl)furan-2-boronic acid pinacol ester
95%
- Product Code: 89994
CAS:
2223029-74-9
| Molecular Weight: | 254.08726 g./mol | Molecular Formula: | C₁₂H₁₉BO₅ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This chemical is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for designing molecules with specific biological activities. Its stability and reactivity under mild conditions make it a preferred choice for researchers in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | Ft89,209.61 |
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| 0.025 | 10-20 days | Ft261,810.82 |
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3-(Acetyl)furan-2-boronic acid pinacol ester
This chemical is widely used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for designing molecules with specific biological activities. Its stability and reactivity under mild conditions make it a preferred choice for researchers in synthetic chemistry.
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