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Structure of 1313399-68-6
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7-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one features a brominated isoquinoline core with a methyl substituent at the 2-position, enabling selective functionalization in synthetic routes. The lactam moiety enhances solubility and stability under standard conditions, while the electron-withdrawing bromine facilitates cross-coupling reactions. This scaffold serves as a key building block for bioactive molecule synthesis.
7-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one serves as a versatile scaffold for medicinal chemistry and synthetic organic applications. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the ketone functionality supports nucleophilic additions and reductive transformations. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate efficient derivatization in drug discovery workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: