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Structure of 20780-75-0
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4-Iodoindoline-2,3-dione serves as a reactive electrophilic scaffold for C–H functionalization and cross-coupling processes. The iodine atom enables efficient palladium-catalyzed transformations, while the fused diketone core provides rigidity and enhanced stability under standard conditions. This structure facilitates direct derivatization at the indoline nitrogen and adjacent positions, enabling rapid access to complex heterocyclic architectures in medicinal chemistry and materials science applications.
4-Iodoindoline-2,3-dione serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its stable iodide functionality. The molecule’s electron-deficient indoline scaffold facilitates electrophilic functionalization and provides a robust platform for constructing complex heterocyclic frameworks. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for iterative synthesis and medicinal chemistry applications.
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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: