(2-((3,4-Dihydroquinolin-1(2H)-yl)methyl)phenyl)boronic acid
95%
Reagent
Code: #41128
CAS Number
1332336-18-1
blur_circular Chemical Specifications
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Molecular Information
Weight
267.13062 g/mol
Formula
C₁₆H₁₈BNO₂
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent. It is employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a quinoline moiety, also makes it suitable for applications in medicinal chemistry, where it can be used to develop bioactive molecules or as a building block for drug discovery. Additionally, it may serve as a ligand or intermediate in the synthesis of complex organic compounds.
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