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Structure of 4334-88-7
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Reactant involved in:Oxidative hydroxylation for the preparation of phenolsHomolytic aromatic substitutionCross-coupling with -bromocarbonyl compoundsSuzuki-coupling reaction with quinoline carboxylatesTrifluoromethylationCarbometalation of ynamides
4-(Ethoxycarbonyl)phenylboronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient construction of biaryl scaffolds with high functional group tolerance. The ethoxycarbonyl group provides stability and facilitates downstream derivatization, while the boronic acid moiety ensures reliable reactivity under mild conditions. Its bench-stable solid form simplifies handling and purification, making it ideal for iterative synthesis in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: