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Structure of 797755-11-4
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This boronate-functionalized propanoic acid integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, offering robust stability under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety enables efficient palladium-catalyzed bond formation, while the carboxylic acid group provides a versatile handle for further derivatization in synthetic and medicinal chemistry applications.
3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoic acid serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The sterically hindered tetramethylboronate group ensures excellent stability under ambient conditions and facilitates efficient palladium-catalyzed coupling with aryl halides and triflates. Its carboxylic acid functionality enables direct derivatization or incorporation into bioactive scaffolds, offering broad utility in medicinal chemistry and materials synthesis.
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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: