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Structure of 552330-86-6
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5-Bromo-2,3-dihydro-1H-isoindol-1-one features a brominated isoindolinone core with enhanced electrophilicity at the carbonyl carbon. This bench-stable scaffold integrates readily into C–H functionalization and transition-metal-catalyzed coupling reactions. The electron-deficient ring system facilitates nucleophilic addition and enables access to complex heterocyclic architectures in medicinal chemistry and materials synthesis.
5-Bromo-2,3-dihydro-1H-isoindol-1-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C5 position via palladium-catalyzed cross-coupling reactions. The isoindolinone core provides structural rigidity and favorable pharmacophoric properties, while the bromide facilitates efficient diversification. Bench-stable and compatible with standard synthetic protocols, it functions effectively in the construction of complex heterocyclic scaffolds and API intermediates.
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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-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P341-P312-P330-P363-P501
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Lot numbers can be found on the outside label of a product: