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Structure of 99-42-3
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Methyl 4-hydroxy-3-nitrobenzoate features a strategically positioned hydroxyl group and electron-withdrawing nitro moiety on the aromatic ring, enabling precise tuning of reactivity in synthetic transformations. This bench-stable compound integrates readily into complex molecular architectures, particularly in medicinal chemistry scaffolds requiring balanced polarity and metabolic stability.
Methyl 4-hydroxy-3-nitrobenzoate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling the construction of bioactive heterocycles and functionalized aromatic scaffolds. The ortho-directed nitro and hydroxyl groups facilitate selective transformations, while the ester functionality supports derivatization via hydrolysis or nucleophilic substitution. Bench-stable and readily purified by recrystallization, it functions reliably in standard coupling and reduction protocols.
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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-H335
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Precautionary Statements : P261-P280-P304+P340
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Lot numbers can be found on the outside label of a product: