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Structure of 19499-93-5
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2,3-Dimethyl-4-nitrophenol features a nitro group at the para position relative to the phenolic hydroxyl, enhancing electrophilic reactivity. The adjacent methyl substituents provide steric protection and improve bench stability. This configuration enables selective functionalization in synthetic sequences requiring electron-deficient aromatic platforms.
2,3-Dimethyl-4-nitrophenol serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering a readily accessible ortho-substituted nitrophenol scaffold. Its stability under standard handling conditions and compatibility with common functional group transformations—such as reduction to the corresponding amine or coupling reactions—facilitate downstream derivatization. The molecule’s defined regiochemistry enables predictable reactivity in electrophilic substitution and transition-metal-catalyzed cross-coupling processes, making it a practical choice for constructing complex aromatic systems.
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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 : H315-H319
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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: