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Structure of 90564-26-4
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Methyl 2-methoxy-3-nitrobenzoate features a nitro group positioned ortho to the ester, enhancing electrophilicity for nucleophilic substitution. The methoxy substituent provides electron-donating character, modulating reactivity in cross-coupling and functionalization sequences. This bench-stable derivative serves as a key intermediate in pharmaceutical synthesis and fine chemical development.
Methyl 2-methoxy-3-nitrobenzoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized aromatic scaffolds. The ortho-dinitro substitution pattern facilitates selective transformations, while the methyl ester and methoxy groups provide orthogonal handles for further derivatization. Its bench-stable nature and compatibility with standard coupling and reduction protocols make it well-suited for medicinal chemistry and process development 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: