2-Methyl-4-(piperidin-1-yl)phenylboronic acid
95%
Reagent
Code: #91740
CAS Number
2159136-20-4
blur_circular Chemical Specifications
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Molecular Information
Weight
219.08782 g/mol
Formula
C₁₂H₁₈BNO₂
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Storage & Handling
Storage
-20℃
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to act as a key reagent in forming carbon-carbon bonds, which is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a building block in the synthesis of complex molecules, contributing to the creation of biologically active compounds and polymers. Its stability and reactivity make it a valuable tool in medicinal chemistry for drug discovery and development.
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2-Methyl-4-(piperidin-1-yl)phenylboronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables it to act as a key reagent in forming carbon-carbon bonds, which is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it serves as a building block in the synthesis of complex molecules, contributing to the creation of biologically active compounds and polymers. Its stability and reactivity make it a valuable tool in medicinal chemistry for drug discovery and development.
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