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Structure of 15997-89-4
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5,6-Dichloroisoindoline-1,3-dione delivers a highly electron-deficient isoindoline scaffold with enhanced stability under standard conditions. The dual chloro substituents at the 5,6-positions intensify reactivity in cycloaddition and nucleophilic substitution processes. This bench-stable derivative serves as a strategic building block for complex heterocyclic architectures in synthetic methodology and medicinal chemistry applications.
5,6-Dichloroisoindoline-1,3-dione serves as a versatile dienophile in Diels-Alder reactions and functions as a stable, bench-ready building block for heterocyclic synthesis. Its electron-deficient core enables efficient cycloadditions with dienes, facilitating rapid access to complex polycyclic frameworks. The dichloro substitution enhances reactivity while maintaining handling stability, making it well-suited for iterative synthetic sequences in medicinal chemistry and materials science applications.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: