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Structure of 201932-92-5
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Methyl 3-(hydroxymethyl)-4-nitrobenzoate features a nitro group at the para position and a hydroxymethyl substituent at the meta position relative to the ester, providing dual functional handles for downstream derivatization. This bench-stable compound integrates readily into synthetic sequences requiring electron-deficient aromatic intermediates with orthogonal reactivity.
Methyl 3-(hydroxymethyl)-4-nitrobenzoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted benzene derivatives. The nitro group facilitates electrophilic substitution and subsequent reduction to an amine, while the hydroxymethyl function supports oxidation to carboxylic acid or ether formation. Its methyl ester moiety permits selective transformations, and the molecule exhibits good bench stability and ease of purification, making it well-suited for iterative synthesis in 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: