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Structure of 13020-57-0
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This ketone features a hydroxylated aromatic ring paired with a phenyl group, delivering enhanced solubility and reactivity. The ortho-hydroxy functionality enables intramolecular hydrogen bonding, stabilizing reactive intermediates. It serves as a key scaffold in the synthesis of bioactive compounds and functional materials.
(3-Hydroxyphenyl)(phenyl)methanone serves as a versatile synthetic building block for aromatic ketones, enabling efficient access to substituted benzophenones and heterocyclic scaffolds. Its hydroxyl group facilitates downstream functionalization via etherification or esterification, while the ketone functionality supports nucleophilic additions and condensation reactions. Bench-stable and readily purified by recrystallization, it functions effectively in standard organic transformations.
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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-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: