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Structure of 6344-05-4
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4-Chloroindoline-2,3-dione features a chlorinated indoline core with two adjacent carbonyl groups, delivering high reactivity in cycloaddition and electrophilic substitution reactions. This electron-deficient scaffold integrates readily into complex heterocyclic architectures under mild conditions.
4-Chloroindoline-2,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted indole scaffolds via cycloaddition and condensation reactions. Its electrophilic C4-chloro group facilitates nucleophilic substitution under mild conditions, while the diketone moiety supports enolization and cyclization pathways. The compound exhibits good bench stability and compatibility with common functional groups, making it suitable for use in medicinal chemistry campaigns targeting heterocyclic libraries and API intermediates.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H319
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Precautionary Statements : P264-P270-P280-P305+P351+P338-P330-P405-P501
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Lot numbers can be found on the outside label of a product: