3-Ethoxycarbonylphenylboronic acid pinacol ester
97%
- Product Code: 90118
Alias:
3-Ethoxycarbonylphenylboronic acid pinacol ester
Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
3-Carbonethoxyphenylboronic acid pinacol ester
CAS:
269410-00-6
| Molecular Weight: | 276.14 g./mol | Molecular Formula: | C₁₅H₂₁BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03093896 | |
| Melting Point: | 40-44 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
3-Ethoxycarbonylphenylboronic acid pinacol ester is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate for constructing complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive compounds and functionalized polymers, where precise molecular architecture is essential. The ethoxycarbonyl group further enhances its versatility, allowing for subsequent chemical modifications to tailor properties for specific applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿270.00 |
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| 1.000 | 10-20 days | ฿657.00 |
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| 5.000 | 10-20 days | ฿2,169.00 |
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3-Ethoxycarbonylphenylboronic acid pinacol ester
3-Ethoxycarbonylphenylboronic acid pinacol ester is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate for constructing complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of bioactive compounds and functionalized polymers, where precise molecular architecture is essential. The ethoxycarbonyl group further enhances its versatility, allowing for subsequent chemical modifications to tailor properties for specific applications.
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