13565-43-0

Basic information

• Product Name: 2-Propen-1-one, 1-(2-methylphenyl)-3-phenyl-, (2E)-
• CAS NO: 13565-43-0
• Molecular Formula: C16H14O
• Molecular Weight: 222.287
• Mol File: 13565-43-0.mol
• Article Data: 37

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-(2-methylphenyl)-3-phenyl-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-(2-methylphenyl)-3-phenyl-, (2E)-(13565-43-0)
• EPA Substance Registry System: 2-Propen-1-one, 1-(2-methylphenyl)-3-phenyl-, (2E)-(13565-43-0)

Safety Data

• Hazardous Substances Data: 13565-43-0(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 577-16-2 2-Methylacetophenone 
• 479213-83-7 1-(2-methylphenyl)-3-phenyl-prop-2-yn-1-ol 
• 536-74-3 phenylacetylene 
• 529-20-4 2-methylphenyl aldehyde 
• 100-51-6 benzyl alcohol 
• 5153-67-3 nitrostyrene 
• 100-42-5 styrene 
• 140-10-3 (E)-3-phenylacrylic acid 
• 766-47-2 1-ethynyl-2-methylbenzene 
• 615-37-2 ortho-methylphenyl iodide 
• 201230-82-2 carbon monoxide 
• 7287-82-3 1-O-tolyl-ethanol 
• 1234571-83-5 3-hydroxy-1-(2-methylphenyl)-3-phenylpropan-1-one 

Downstream Products

• 918665-18-6 1-(2-methyl-phenyl)-3-phenyl-2,3-epoxy-1-propanone 
• 1384192-11-3 (R)-3-phenyl-1-o-tolylpentan-1-one 
• 1384191-96-1 (S)-3-phenyl-1-o-tolylpentan-1-one 
• 93433-65-9 1-(2-methylphenyl)-3-phenyl-1-propanone 
• 94211-96-8 2-methyl-4,6-diphenylpyridine-3-carbonitrile 
• 87116-43-6 [5-(2-Methyl-benzoyl)-2,4-diphenyl-tetrahydro-thiophen-3-yl]-o-tolyl-methanone 
• 92208-76-9 (2-Methylphenyl)(c-2,t-3-diphenylcycloprop-r-1-yl)methanon 
• 92208-76-9 (2-Methylphenyl)(t-2,t-3-diphenylcycloprop-r-1-yl)methanon 
• 125877-46-5 5-Methyl-4-phenyl-2-o-tolyl-pyridine 

Relevant articles and documents

A Facile FeCl3/I2-Catalyzed Aerobic Oxidative Coupling Reaction: Synthesis of Tetrasubstituted Imidazoles from Amidines and Chalcones

A facile and efficient route for the synthesis of tetrasubstituted imidazoles from amidines and chalcones via FeCl3/I2-catalyzed aerobic oxidative coupling has been developed. This new strategy is featured by high regioselectivity an

Palladium-Catalyzed Synthesis of α-Methyl Ketones from Allylic Alcohols and Methanol

One-pot synthesis of α-methyl ketones starting from 1,3-diaryl propenols or 1-aryl propenols and methanol as a C1 source is demonstrated. This one-pot isomerization-methylation is catalyzed by commercially available Pd(OAc)2 with H2O as the only by-product. Mechanistic studies and deuterium labelling experiments indicate the involvement of isomerization of allyl alcohol followed by methylation through a hydrogen-borrowing pathway in these isomerization-methylation reactions.

Iridium and copper supported on silicon dioxide as chemoselective catalysts for dehydrogenation and borrowing hydrogen reactions

High active ligand usually plays an important role during catalysis and synthesis chemistry. A new and efficient benzotriazole-pyridinyl-silane ligand (BPS) was designed, and the corresponding iridium and copper catalysts were synthesized and thoroughly characterized by means of EDS, TEM, and XPS. The resulting iridium composite revealed excellent catalytic activity for the reaction of tert-butanesulfinamide with benzyl alcohols, while copper catalyst could realize the synthesis of unsaturated carbonyl compounds through the reaction of benzyl alcohols with ketones. This provided an efficient method for selective synthesis of unsaturated carbonyl compounds from benzyl alcohols and ketones in high yields with good recovery performance.