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Structure of 2150-43-8
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Methyl 3,4-dihydroxybenzoate features two adjacent hydroxyl groups on the aromatic ring, enhancing solubility and reactivity in synthetic transformations. This ortho-dihydroxy motif enables efficient metal chelation and serves as a key scaffold in bioactive molecule design. The methyl ester group offers stability under standard conditions while permitting selective hydrolysis for downstream derivatization.
Methyl 3,4-dihydroxybenzoate serves as a versatile building block in synthetic organic chemistry, enabling access to bioactive phenolic scaffolds and natural product analogs. Its ortho-dihydroxy functionality facilitates oxidation to quinones, complexation with metals, and derivatization under standard conditions. The methyl ester group provides stability and compatibility with diverse transformations, including hydrogenation, nucleophilic substitution, and coupling reactions. This compound exhibits excellent bench stability and ease of purification, making it well-suited for medicinal chemistry campaigns 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: