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Structure of 1677-48-1
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5,6-Dichloroindoline-2,3-dione features a rigid, electron-deficient indoline scaffold bearing two chlorine substituents at the 5 and 6 positions. This configuration enhances electrophilicity at the carbonyl-rich core, enabling efficient coupling in transition-metal-catalyzed cross-coupling reactions. The compound exhibits excellent bench stability and solubility in common organic solvents, facilitating its use in synthetic workflows requiring reactive heterocyclic intermediates.
5,6-Dichloroindoline-2,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to chlorinated heterocyclic scaffolds. Its reactive diketone core facilitates electrophilic substitution and cycloaddition reactions, while the dichloro substitution enhances stability and modulates reactivity. The compound functions effectively in the synthesis of medicinally relevant indole derivatives and offers robust performance in standard bench-scale transformations.
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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: