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Structure of 269409-74-7
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3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid features a boronate ester group enabling reliable Suzuki-Miyaura coupling under mild conditions. The carboxylic acid functionality offers direct handle for derivatization, while the tetramethyl-substituted dioxaborolane enhances stability and shelf life. This ortho-functionalized scaffold integrates seamlessly into complex molecular architectures.
3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid serves as a versatile boronate building block in Suzuki-Miyaura cross-coupling reactions. The pinacol boronate ester group enables efficient C–C bond formation under mild conditions, while the carboxylic acid functionality provides a handle for derivatization or conjugation. Bench-stable and compatible with a wide range of functional groups, it facilitates rapid access to substituted biaryls and complex heterocyclic scaffolds 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: