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Structure of 13494-10-5
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This phenolic ketone features two adjacent hydroxyl groups on the aromatic ring, enhancing solubility and enabling facile derivatization. The acetyl functionality provides a reactive handle for conjugation or further functionalization in synthetic pathways. Stable under standard bench conditions, it serves as a key intermediate in bioactive molecule synthesis.
1-(2,3-Dihydroxyphenyl)ethanone serves as a versatile building block for catechol-containing scaffolds, enabling efficient synthesis of bioactive molecules through established coupling and oxidation protocols. Its ortho-dihydroxy functionality supports metal chelation and facilitates downstream functionalization, while the ketone group offers direct access to enantioselective transformations. Bench-stable and compatible with standard purification methods, it functions reliably in medicinal chemistry campaigns requiring phenolic motifs.
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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: