2657-24-1

Basic information

• Product Name: 1-Propanone, 1-(4-methoxyphenyl)-3,3-diphenyl-
• CAS NO: 2657-24-1
• Molecular Formula: C22H20O2
• Molecular Weight: 316.4
• Mol File: 2657-24-1.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 1-(4-methoxyphenyl)-3,3-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 1-(4-methoxyphenyl)-3,3-diphenyl-(2657-24-1)
• EPA Substance Registry System: 1-Propanone, 1-(4-methoxyphenyl)-3,3-diphenyl-(2657-24-1)

Safety Data

• Hazardous Substances Data: 2657-24-1(Hazardous Substances Data)

Usage

Uses

Fragrance and flavor ingredient in perfumes, soaps, and cosmetics; photoinitiator in UV-curing applications; sunscreen agent in sun care products; chemical intermediate in the synthesis of pharmaceuticals and other organic compounds

Safety

Relatively safe for use in consumer products when used in accordance with regulatory guidelines, but proper handling and storage is necessary to prevent potential hazards.

Upstream product

• 959-23-9 4'-methoxychalcone 
• 22966-19-4 trans-4'-methoxychalcone 
• 99354-16-2 phenylcerium dichloride 
• 30925-53-2 (2Z)-1-(4-methoxyphenyl)-3-phenylprop-2-en-1-one 
• 591-51-5 phenyllithium 
• 37089-77-3 3,3-diphenylpropanoyl chloride 
• 100-66-3 methoxybenzene 
• 91-01-0 1,1-Diphenylmethanol 
• 768-60-5 4-methoxyphenylacetylen 
• 98-80-6 phenylboronic acid 
• 101-81-5 Diphenylmethane 
• 22390-98-3 1-(4-methoxyphenyl)ethenyl acetate 
• 853-83-8 N-tosyldiphenylmethylamine 
• 13422-77-0 3-(4-methoxy-phenyl)-3-oxo-propionic acid 

Downstream Products

• 129919-64-8 (E,Z)-1-(4-Methoxyphenyl)-3,3-diphenylpropene 
• 115679-97-5 1,1-Bis(4-methoxyphenyl)-3,3-diphenylpropene 
• 129919-65-9 1-(4-Methoxyphenyl)-1,trans-2,3-triphenylcyclopropane 
• 129919-67-1 1,1-Bis(4-methoxyphenyl)-trans-2,3-diphenylcyclopropane 
• 129919-66-0 <(3S,4S,5S)/(3R,4R,5R)>-3-(4-Methoxyphenyl)-3,4,5-triphenyl-1,2-dioxolane 
• 129919-66-0 <(3S,4S,5R)/(3R,4R,5S)>-3-(4-Methoxyphenyl)-3,4,5-triphenyl-1,2-dioxolane 
• 129919-66-0 <(3R,4S,5R)/(3S,4R,5S)>-3-(4-Methoxyphenyl)-3,4,5-triphenyl-1,2-dioxolane 
• 129919-66-0 <(3R,4S,5S)/(3S,4R,5R)>-3-(4-Methoxyphenyl)-3,4,5-triphenyl-1,2-dioxolane 
• 129919-68-2 3,3-Bis(4-methoxyphenyl)-cis-4,5-diphenyl-1,2-dioxolane 
• 129919-68-2 3,3-Bis(4-methoxyphenyl)-trans-4,5-diphenyl-1,2-dioxolane 
• 1443368-03-3 1-(1-(4-methoxyphenyl)-3,3-diphenylpropylidene)-2-phenylhydrazine 
• 1443367-63-2 3-(4-methoxyphenyl)-1,5,5-triphenyl-4,5-dihydro-1H-pyrazole 
• 1443368-04-4 N'-(1-(4-methoxyphenyl)-3,3-diphenylpropylidene)benzohydrazide 
• 1443367-64-3 (3-(4-methoxyphenyl)-5,5-diphenyl-4,5-dihydro-1H-pyrazol-1-yl)(phenyl)methanone 

Relevant articles and documents

β-phenyl quenching of triplet excited ketones: How critical is the geometry for deactivation?

The phenomenon of β-phenyl quenching has been examined by laser-flash photolysis in a series of α- and/or β-substituted ketones 4-8 with similar excited-state characteristics. It is found that α-substitution markedly increases the triplet lifetimes in con

Microwave-Assisted Condensation of Benzylic Alcohols and Alkynes Promoted by Zinc Halides: Concise Access to Alkenyl Halides

A simple Lewis acid-mediated route for the synthesis of alkenyl halides are described under microwave-assisted conditions. The reaction proceeds through the condensation between secondary alcohols and terminal acetylenes and regioselective hydrohalogenati

Synthesis of β,β-diaryl propiophenones via palladium-catalyzed domino arylboronation, elimination and enone hydroarylation of enaminones

The syntheses of β,β-diaryl aryl propiophenones have been realized via palladium-catalyzed domino reactions of dimethyl amino functionalized enaminones and aryl boronic acids. This is the first example of transition metal-catalyzed enaminone C-N bond conversion for the generation of a new C-C(aryl) structure.