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Structure of 1193-54-0
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3,4-Dichloro-1H-pyrrole-2,5-dione features a highly electron-deficient pyrrolinedione core with chlorine substituents at the 3- and 4-positions, enhancing its reactivity in cycloaddition and electrophilic substitution processes. This bench-stable compound serves as a key building block in heterocyclic synthesis, particularly for constructing complex nitrogen-containing frameworks under mild conditions.
3,4-Dichloro-1H-pyrrole-2,5-dione serves as a versatile dienophile in Diels-Alder reactions and functions as a key building block for heterocyclic scaffolds. Its electron-deficient pyrrolinedione core enables efficient cycloadditions with dienes, offering high regioselectivity and stability under standard reaction conditions. The dichloro substitution enhances reactivity while maintaining bench stability, facilitating straightforward purification and integration into synthetic sequences targeting complex molecular architectures.
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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: