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Structure of 1075719-87-7
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2-(4-Ethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a bench-stable boronate ester featuring a para-ethyl-substituted aryl group. This structure enables efficient coupling in palladium-catalyzed cross-coupling reactions, offering reliable reactivity and ease of handling under standard conditions.
2-(4-Ethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its tetramethyl-substituted dioxaborolane core enhances air and moisture stability while maintaining high reactivity with aryl halides and triflates. The ethyl-substituted phenyl group provides a well-defined aromatic handle for constructing biaryl scaffolds in medicinal chemistry and materials science. Ideal for scalable synthesis and purification via standard chromatographic methods.
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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: