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Structure of 337536-15-9
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4-Bromoisoindolin-1-one features a brominated isoindolinone scaffold with enhanced electrophilic character at the carbonyl carbon. This bench-stable compound integrates readily into transition-metal-catalyzed cross-coupling reactions, enabling efficient access to functionalized heterocycles under mild conditions.
4-Bromoisoindolin-1-one serves as a versatile building block in medicinal chemistry, enabling efficient access to biologically relevant isoindolinone scaffolds. The bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the ketone functionality supports nucleophilic additions and condensation processes. Its bench-stable crystalline form and compatibility with diverse reaction conditions make it well-suited for modular synthesis of drug candidates and functionalized heterocycles.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: