(4-(((1-(tert-butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid (4-(((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid
98%
Reagent
Code: #89168
CAS Number
1224449-13-1
blur_circular Chemical Specifications
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Molecular Information
Weight
335.21 g/mol
Formula
C₁₇H₂₆BNO₅
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Registry Numbers
MDL Number
MFCD28400568
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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 the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperidine moiety, makes it valuable in medicinal chemistry for the development of drug candidates. The Boc group provides stability during synthetic processes, while the boronic acid functionality allows for versatile coupling with aryl or vinyl halides. This compound is often employed in the preparation of biologically active molecules, including pharmaceuticals and agrochemicals, where precise control over molecular architecture is essential. Additionally, its application extends to materials science, where it contributes to the design of advanced organic materials with tailored properties.
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(4-(((1-(tert-butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid (4-(((1-(tert-Butoxycarbonyl)piperidin-4-yl)oxy)methyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protected piperidine moiety, makes it valuable in medicinal chemistry for the development of drug candidates. The Boc group provides stability during synthetic processes, while the boronic acid functionality allows for versatile coupling with aryl or vinyl halides. This compound is often employed in the preparation of biologically active molecules, including pharmaceuticals and agrochemicals, where precise control over molecular architecture is essential. Additionally, its application extends to materials science, where it contributes to the design of advanced organic materials with tailored properties.
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