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Structure of 1313399-69-7
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2-Methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinolin-1(2H)-one features a boronate ester handle integrated into a sterically hindered dihydroisoquinolinone scaffold. This structure enables efficient Suzuki–Miyaura cross-coupling under mild conditions, delivering complex heterocyclic architectures with high functional group tolerance and bench-stable handling.
2-Methyl-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 palladium-catalyzed cross-coupling reactions. Its dihydroisoquinolinone core provides structural rigidity and functional group compatibility, enabling efficient diversification in medicinal chemistry. The pinacol boronate ester offers excellent stability, ease of handling, and compatibility with standard Suzuki-Miyaura conditions, facilitating rapid access to complex heterocyclic scaffolds.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: