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Structure of 63603-09-8
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Methyl 4-chloro-3-methoxy-5-nitrobenzoate features a nitro group at the para position relative to the ester, enhancing electrophilicity for downstream functionalization. The chloro and methoxy substituents provide orthogonal reactivity and solubility balance. This bench-stable derivative serves as a key intermediate in medicinal chemistry scaffolds and heterocyclic synthesis under standard conditions.
Methyl 4-chloro-3-methoxy-5-nitrobenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling regioselective functionalization via its complementary electron-withdrawing nitro and chloro groups. The methoxy group provides ortho-directed reactivity, while the ester functionality supports subsequent transformations such as hydrolysis, reduction, or coupling reactions. Its bench-stable nature and compatibility with standard cross-coupling protocols facilitate efficient access to substituted aromatic scaffolds.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P304+P341-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: