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Structure of 603122-40-3
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Methyl 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate delivers a boronate ester functionality paired with an electron-rich aromatic core. This bench-stable reagent integrates seamlessly into Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under standard conditions. The tetramethyl-substituted dioxaborolane moiety enhances stability and minimizes protodeboronation, while the methoxy group fine-tunes electronic properties for predictable reactivity.
Methyl 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The sterically protected boronate group enables high stability under ambient conditions and facilitates efficient coupling with aryl halides and triflates. Its methoxy and methyl ester functionalities provide orthogonal reactivity for downstream derivatization, making it well-suited for the synthesis of complex aromatic scaffolds in medicinal chemistry and materials science.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: