(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
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CAS Number 1224449-13-1

blur_circular Chemical Specifications

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Weight 335.21 g/mol
Formula C₁₇H₂₆BNO₅
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MDL Number MFCD28400568
inventory_2 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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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,430.00
(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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