50793-44-7

Basic information

• Product Name: 2-Propen-1-one, 2-bromo-3-(4-methoxyphenyl)-1-phenyl-
• CAS NO: 50793-44-7
• Molecular Formula: C16H13BrO2
• Molecular Weight: 317.182
• Mol File: 50793-44-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 2-bromo-3-(4-methoxyphenyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 2-bromo-3-(4-methoxyphenyl)-1-phenyl-(50793-44-7)
• EPA Substance Registry System: 2-Propen-1-one, 2-bromo-3-(4-methoxyphenyl)-1-phenyl-(50793-44-7)

Safety Data

• Hazardous Substances Data: 50793-44-7(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 98-86-2 acetophenone 
• 22252-15-9 trans-4-methoxychalcone 
• 10325-67-4 2,3-dibromo-3-(4-methoxy-phenyl)-1-phenyl-propan-1-one 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 50999-22-9 3-ethoxy-2-bromo-3-(4-methoxy-phenyl)-1-phenyl-propan-1-one 
• 90399-67-0 2-bromo-3-methoxy-3-(4-methoxy-phenyl)-1-phenyl-propan-1-one 
• 64-17-5 ethanol 

Downstream Products

• 135549-14-3 8-(4-Methoxy-phenyl)-6-phenyl-3-propyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine 
• 1221289-08-2 C₂₄H₁₈O₂ 
• 1214892-12-2 C₂₅H₁₇ClN₂O₂S 
• 65-85-0 benzoic acid 
• 3672-51-3 5-(4-methoxyphenyl)-3-phenylisoxazole 
• 135549-19-8 3-(2-Chloro-phenoxymethyl)-8-(4-methoxy-phenyl)-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine 
• 135549-17-6 3-(4-Chloro-phenoxymethyl)-8-(4-methoxy-phenyl)-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine 
• 135549-15-4 8-(4-Methoxy-phenyl)-3,6-diphenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine 
• 135549-13-2 3-Ethyl-8-(4-methoxy-phenyl)-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine 
• 135549-12-1 8-(4-Methoxy-phenyl)-3-methyl-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine 
• 135549-11-0 8-(4-Methoxy-phenyl)-6-phenyl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazepine 

Relevant articles and documents

Modular access to 1,2-allenyl ketones based on a photoredox-catalysed radical-polar crossover process

Herein, a new protocol dealing with the preparation of 1,2-allenyl ketones has been successfully developedviathe reactions of enynes with radicals enabled by dual photoredox/copper catalysis. Based on the results of a deuteration experiment and the competition reaction between cyclopropanation and allenation, the mechanism based on a photoredox-neutral-catalysed radical-polar crossover process has been proposed. Synthetic applications of allenes have also been demonstrated.

Sc(OTf)3-Catalyzed Diastereoselective Formal [3+2] Cycloaddition Reactions of Alkynylcyclopropane Ketones with Electron-Rich Aromatic Aldehydes to Yield 2,5-trans-Tetrahydrofurans

In contast to the general [4+2] cycloaddition reactions of alkynylcyclopropane ketones reported in the literature, we report herein a Sc(OTf)3-catalyzed formal intermolecular [3+2] cycloaddition reaction of alkynylcyclopropane ketones with elec

New Derivatives of N-Vinyltriazoles: 1,3-Diaryl-3-(1H-1,2,4-triazol-1-yl)-2-propen-1-ones

We have synthesized previously unknown N-vinyltriazoles: 1,3-diaryl-3-(1H-1,2,4-triazol-1-yl)-2-propen-1-ones.We discusss a hypothesis for a probable reaction mechanism.