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Structure of 827-33-8
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4-Bromo-5-chloro-2-nitroaniline features a highly functionalized aromatic core with complementary halogen and nitro groups, enabling direct coupling in cross-coupling reactions. The electron-deficient ring facilitates nucleophilic substitution, while the ortho-halogen positions support selective Pd-catalyzed transformations. This compound serves as a key intermediate in the synthesis of advanced pharmaceuticals and agrochemicals requiring precise substitution patterns.
4-Bromo-5-chloro-2-nitroaniline serves as a versatile building block for the synthesis of heterocyclic scaffolds and functionalized aromatic compounds. Its complementary halogen and nitro groups enable sequential cross-coupling, nucleophilic substitution, and reduction strategies under standard reaction conditions. The molecule exhibits bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns and API intermediate 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-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: