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Structure of 80166-90-1
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5-Bromo-7-nitroindoline delivers a sterically accessible indoline scaffold bearing a bromine at the 5-position and a nitro group at the 7-position, enabling direct functionalization in cross-coupling and electrophilic substitution reactions. This electron-deficient heterocycle facilitates efficient derivatization under standard conditions.
5-Bromo-7-nitroindoline serves as a versatile building block for the synthesis of functionalized indoline scaffolds, enabling direct C–H functionalization and cross-coupling reactions. Its bromo and nitro groups provide orthogonal reactivity for palladium-catalyzed transformations and selective reduction sequences, facilitating access to complex heterocycles. The compound exhibits good bench stability and is amenable to standard purification techniques, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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-H312-H315-H319-H332-H335-H402
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Precautionary Statements : P260-P261-P264-P270-P271-P273-P280-P301+P310-P302+P352-P304+P341-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: