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Structure of 1231892-74-2
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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinolin-1(2H)-one features a boronate ester group enabling direct Suzuki-Miyaura coupling under mild conditions. The dihydroisoquinolinone core provides a rigid, electron-rich scaffold suitable for bioactive molecule synthesis. Bench-stable and moisture-tolerant, this reagent streamlines the construction of complex heterocycles in medicinal chemistry and materials science workflows.
7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinolin-1(2H)-one serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylborolane moiety enables stable, air-tolerant handling and broad functional group compatibility. It facilitates efficient construction of biaryl and heteroaryl architectures in medicinal chemistry and materials synthesis, with the dihydroisoquinolinone core providing a scaffold relevant to CNS-targeted compounds and kinase inhibitors.
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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: