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Structure of 827-23-6
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2,4-Dibromo-6-nitroaniline features a highly electron-deficient aromatic core due to dual bromine substituents and a nitro group at the para position. This configuration enables direct incorporation into cross-coupling reactions under mild conditions. The molecule exhibits enhanced stability and resistance to premature decomposition, facilitating reliable use in synthetic sequences requiring precise functional group compatibility.
2,4-Dibromo-6-nitroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct substitution at the nitro and amino positions. Its bromine atoms facilitate palladium-catalyzed cross-coupling reactions, while the electron-withdrawing nitro group enhances electrophilicity for nucleophilic aromatic substitution. The compound exhibits bench stability and is compatible with standard purification techniques, making it a practical intermediate for constructing complex heterocyclic scaffolds and functionalized aryl systems.
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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+H332-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: