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Structure of 7138-15-0
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3-Bromo-2-nitroaniline features a bromine substituent flanked by a nitro group and an amino moiety, creating a uniquely electron-deficient aromatic system. This trifunctional scaffold enables direct coupling in cross-coupling reactions and facilitates the synthesis of complex heterocycles under mild conditions.
3-Bromo-2-nitroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the aromatic ring through palladium-catalyzed cross-coupling reactions. Its bromo group facilitates efficient C–C and C–N bond formation, while the nitro group provides strong electron-withdrawing character and ortho-directing capability. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for multi-step synthesis workflows.
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GHS No : GHS07,GHS09
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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-H410
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Precautionary Statements : P260-P261-P264-P270-P271-P273-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P391-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: