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Structure of 2137975-62-1
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4-Chloro-3-methoxy-5-nitrobenzamide features a trifunctional aromatic core with orthogonal reactivity: a chloro group enables palladium-catalyzed coupling, the methoxy moiety offers steric and electronic modulation, and the nitro group provides strong electron-withdrawal. This combination facilitates integration into complex molecular architectures under standard conditions.
4-Chloro-3-methoxy-5-nitrobenzamide serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the aromatic ring due to its complementary electron-withdrawing nitro and chloro groups. The methoxy group provides orthogonal handle for selective derivatization, while the amide functionality offers stability and compatibility with standard coupling reactions. Its bench-stable nature and predictable reactivity facilitate efficient synthesis of heterocyclic scaffolds and API intermediates in multi-step routes.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: