79877-07-9

Usage

Uses

Used in Cosmetic Industry:
Ethanone, 1-(3-benzoyl-2-hydroxy-5-methylphenyl)is used as a UV filter for its capacity to absorb and block harmful ultraviolet (UV) radiation from the sun, thereby protecting the skin from sunburn and premature aging.
Used in Skincare Products:
Ethanone, 1-(3-benzoyl-2-hydroxy-5-methylphenyl)is utilized as an antioxidant in skincare formulations to help protect the skin from damage caused by free radicals, which are molecules that can cause cell damage and contribute to aging and other skin conditions.
Used in Anti-Inflammatory Agents:
Ethanone, 1-(3-benzoyl-2-hydroxy-5-methylphenyl)is employed as an anti-inflammatory agent to help reduce redness and swelling in the skin, providing relief for conditions such as dermatitis and other inflammatory skin disorders.
Overall, Ethanone, 1-(3-benzoyl-2-hydroxy-5-methylphenyl)is a multifunctional compound that plays a significant role in the development of various skincare products, enhancing their effectiveness in protecting and maintaining skin health.

Upstream product

• 4010-19-9 1-(2-benzoyloxy-5-methylphenyl)-ethanone 
• 1450-72-2 5-methyl-2-hydroxyacetophenone 
• 98-88-4 benzoyl chloride 
• 1470-57-1 2-hydroxy-5-methylbenzophenone 
• 106-44-5 p-cresol 
• 135564-55-5 2-acetoxy-5-methyl-benzophenone 

Downstream Products

• 133363-99-2 1-(2,3-Dibenzoyl-5-methyl-phenyl)-ethanone 
• 133363-93-6 Benzoic acid [1-(3-benzoyl-2-hydroxy-5-methyl-phenyl)-eth-(E)-ylidene]-hydrazide 
• 133363-96-9 1-(2-Acetyl-6-benzoyl-4-methyl-phenyl)-ethanone 
• 133363-90-3 Acetic acid [1-(3-benzoyl-2-hydroxy-5-methyl-phenyl)-eth-(E)-ylidene]-hydrazide 
• 133363-98-1 1-[3-Benzoyl-5-methyl-2-(4-nitro-benzoyl)-phenyl]-ethanone 
• 86373-13-9 Cu₂(C₉H₅O₃(C₆H₅)CH₃)2⁽²⁺⁾*2(ClO₄)^(1-)*2H₂O=Cu₂(C₉H₅O₃(C₆H₅)CH₃)2(ClO₄)2*2H₂O 
• 133363-91-4 Isonicotinic acid [1-(3-benzoyl-2-hydroxy-5-methyl-phenyl)-eth-(E)-ylidene]-hydrazide 
• 133363-97-0 1-[3-Benzoyl-5-methyl-2-(pyridine-4-carbonyl)-phenyl]-ethanone 
• 86373-04-8 Cu(C₉H₅O₃(C₆H₅)CH₃)2*H₂O 

Relevant academic research and scientific papers

A novel and facile synthesis of 1,2,3-triacylbenzenes

3,4,5-Triacyltoluenes 7 were prepared in high yield by a novel oxidative cleavage reaction of 2,6-diacylcresol monohydrazone 6 with lead tetraacetate.

Dinuclear Metal Complexes. Part 2. Synthesis, Characterisation, and Electrochemical Studies of Macrocyclic Dicopper(II) Complexes

The synthesis, characterisation, and electrochemical studies of dicopper(II) complexes 1>2.nH2O of the macrocycle 7,11;19,23-dimetheno-9,21-dimethyl-tetra-azacycloicosa-5,7,9,12,17,19,21,24-octaene-25,26-diol (H2L1), and of some 6,12,18,24-substituted (Me4; Prn4; Ph4; Ph, Me, Ph, Me) derivatives have been carried out.These compounds undergo sequential one-electron transfers at two different potentials.For all of these compounds, except for 1>2.2H2O, two reversible or almost reversible reduction steps have been observed in acetonitrile medium using a hanging mercury drop electrode.In the case of 1>2.2H2O, the second couple became obscured due to the presence of an adsorption phenomenon or secondary electrode reaction.However, in NN-dimethylformamide (dmf) medium, satisfactory voltammograms have been obtained only with 1>2.2H2O.The mixed-valent complexes are considerably more stable in acetonitrile than is IICuIL1>+ in dmf.The potentials of the first reduction step (E1) remain practically invariant throughout the series and are independent of the extent of magnetic interactions in the dicopper(II) complexes.The potentials of the second reduction step (E2) vary with the alkyl and aryl groups present, and a linear plot has been obtained for E2 vs. the Hammett function ?m.On the basis of previously reported observations and the present study it is inferred that in acetonitrile medium the unpaired electron in the mixed-valent complexes remains localised on one of the copper atoms.