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Structure of 6941-75-9
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5-Bromoisoindoline-1,3-dione features a brominated isoindoline-1,3-dione core with enhanced electrophilicity at the C5 position, enabling efficient coupling in transition-metal-catalyzed reactions. The electron-deficient quinone moiety facilitates conjugation and stability under standard conditions, while the bromine substituent serves as a reliable handle for further functionalization via cross-coupling or nucleophilic substitution. This compound integrates seamlessly into complex molecular architectures requiring precise regiocontrol and reactive site availability.
5-Bromoisoindoline-1,3-dione serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the C5 position via palladium-catalyzed cross-coupling reactions. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for constructing complex heterocyclic scaffolds relevant to medicinal chemistry and materials science. The molecule functions as a robust dienophile in cycloadditions and provides a reliable platform for late-stage diversification in API development 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 : 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: