3-[2-(Dimethylamino)ethoxy]phenylboronic Acid Pinacol Ester
≥95%
Reagent
Code: #90107
CAS Number
925940-40-5
blur_circular Chemical Specifications
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Molecular Information
Weight
291.19 g/mol
Formula
C₁₆H₂₆NO₃B
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Registry Numbers
MDL Number
MFCD09746202
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Storage & Handling
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The dimethylaminoethoxy group enhances solubility and reactivity in various solvents, facilitating its use in diverse reaction conditions. Additionally, it serves as a key intermediate in the development of bioactive compounds and materials with specific electronic or structural properties. Its stability and compatibility with a range of reagents make it a versatile tool in medicinal chemistry and material science research.
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3-[2-(Dimethylamino)ethoxy]phenylboronic Acid Pinacol Ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The dimethylaminoethoxy group enhances solubility and reactivity in various solvents, facilitating its use in diverse reaction conditions. Additionally, it serves as a key intermediate in the development of bioactive compounds and materials with specific electronic or structural properties. Its stability and compatibility with a range of reagents make it a versatile tool in medicinal chemistry and material science research.
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