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Structure of 3416-57-7
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This isoindoline-1,3-dione derivative features a strategically positioned oxopropyl substituent that enhances reactivity in cycloaddition processes. The electron-deficient quinone moiety integrates readily into complex molecular architectures, enabling efficient access to fused polycyclic systems under mild conditions.
2-(2-Oxopropyl)isoindoline-1,3-dione serves as a versatile building block in synthetic organic chemistry, enabling the construction of biologically relevant heterocyclic scaffolds. Its α,β-unsaturated ketone functionality facilitates Michael additions and aldol-type cyclizations under mild conditions. The molecule exhibits good bench stability and is compatible with common protecting group strategies, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: