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Structure of 19727-83-4
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6-Nitroindoline delivers a versatile scaffold for medicinal chemistry, combining a planar indoline core with a nitro group at the 6-position. This electron-deficient moiety enhances reactivity in transition metal-catalyzed couplings and supports photochemical transformations. The compound exhibits bench-stable handling characteristics and integrates readily into complex molecular architectures under standard conditions.
6-Nitroindoline serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the indoline core for late-stage diversification. Its nitro group facilitates selective reduction to an amine, which can be further elaborated via amidation, alkylation, or cyclization reactions. The molecule exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for modular synthesis of heterocyclic scaffolds and potential API intermediates.
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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: