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Structure of 52898-32-5
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This isoindole derivative features a conjugated butenyl side chain enabling efficient coupling in synthetic transformations. The electron-deficient quinoid core enhances reactivity in cycloaddition processes, while the bench-stable structure supports reliable handling under standard conditions.
2-(3-Buten-1-yl)-1H-isoindole-1,3(2H)-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted isoindolinone scaffolds via Pd-catalyzed cross-coupling or conjugate addition reactions. Its α,β-unsaturated lactam moiety exhibits excellent functional group tolerance and bench stability, facilitating straightforward purification and integration into complex molecular architectures relevant to medicinal chemistry and materials science.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: