3-Ethoxycarbonylphenylboronic acid pinacol ester
97%
Reagent
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 Number
269410-00-6
blur_circular Chemical Specifications
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Molecular Information
Weight
276.14 g/mol
Formula
C₁₅H₂₁BO₄
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Registry Numbers
MDL Number
MFCD03093896
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Physical Properties
Melting Point
40-44 °C(lit.)
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Storage & Handling
Storage
Room temperature, dry, sealed
description 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.
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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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