5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinolin-2(1H)-one
95%
Reagent
Code: #42365
CAS Number
1219130-53-6
blur_circular Chemical Specifications
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Molecular Information
Weight
271.1200 g/mol
Formula
C₁₅H₁₈BNO₃
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Registry Numbers
MDL Number
MFCD18427669
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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 Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals and agrochemicals, where the quinolinone moiety can contribute to biological activity. Additionally, it serves as an intermediate in the development of organic materials, including polymers and dyes, due to its ability to introduce functional groups into molecular frameworks.
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