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Structure of 7149-80-6
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5-Chloro-4-methyl-2-nitroaniline features a nitro group at the ortho position relative to an amino handle, enhancing reactivity in coupling processes. The chloro and methyl substituents provide electronic tuning and steric control, enabling selective functionalization in pharmaceutical intermediates and agrochemical synthesis under standard conditions.
5-Chloro-4-methyl-2-nitroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted heterocycles via standard coupling and cyclization protocols. Its nitro group facilitates selective reduction and subsequent functionalization, while the chloro and methyl substituents provide orthogonal reactivity for further diversification. The compound exhibits good bench stability and is amenable to purification by recrystallization or chromatography, making it well-suited for scalable synthetic workflows.
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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: