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Structure of 190367-56-7
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Methyl 4-chloro-2-methyl-5-nitrobenzoate features a conjugated aromatic system bearing electron-withdrawing chloro and nitro groups flanking a methyl ester. This configuration imparts enhanced electrophilicity at the carbonyl carbon, enabling efficient coupling in cross-coupling reactions. The molecule exhibits bench-stable handling characteristics and solubility in common organic solvents, streamlining its integration into synthetic workflows for heterocyclic and pharmaceutical intermediates.
Methyl 4-chloro-2-methyl-5-nitrobenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its ortho-substituted aryl core enables selective functionalization, while the nitro and ester groups provide complementary reactivity for subsequent transformations. The methyl ester facilitates direct coupling or reduction pathways, and the chlorine atom supports palladium-catalyzed cross-coupling reactions. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses requiring predictable regiochemistry and high yield.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: