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Structure of 89-84-9
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2',4'-Dihydroxyacetophenone features a phenolic backbone with strategically positioned hydroxyl groups that enhance solubility and reactivity. This electron-rich scaffold serves as a key intermediate in synthesizing bioactive compounds, particularly those targeting oxidative stress pathways. The molecule exhibits stability under standard bench conditions, enabling straightforward integration into multi-step synthetic sequences.
2',4'-Dihydroxyacetophenone serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted phenolic scaffolds. Its ortho-dihydroxy motif provides enhanced solubility and facilitates metal coordination, while the acetyl group offers a reliable handle for nucleophilic substitution, reduction, or oxidative transformations. This compound exhibits excellent bench stability and is compatible with standard purification methods, making it well-suited for use in medicinal chemistry lead optimization and natural product synthesis 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: