129919-76-2

Basic information

• Product Name: 3-(4-methoxyphenyl)-1,3-diphenyl-1-propanone
• CAS NO: 129919-76-2
• Molecular Weight: 316.4
• Mol File: 129919-76-2.mol
• Article Data: 28

Chemical Properties

• CAS DataBase Reference: 3-(4-methoxyphenyl)-1,3-diphenyl-1-propanone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxyphenyl)-1,3-diphenyl-1-propanone(129919-76-2)
• EPA Substance Registry System: 3-(4-methoxyphenyl)-1,3-diphenyl-1-propanone(129919-76-2)

Safety Data

• Hazardous Substances Data: 129919-76-2(Hazardous Substances Data)

Upstream product

• 60-29-7 diethyl ether 
• 959-33-1 3-(4-methoxyphenyl)-1-phenylprop-2-en-1-one 
• 5720-07-0 4-methoxyphenylboronic acid 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 696-62-8 para-iodoanisole 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 100-52-7 benzaldehyde 
• 98-86-2 acetophenone 
• 94-41-7 benzalacetophenone 
• 3262-89-3 triphenylboroxine 
• 22252-15-9 trans-4-methoxychalcone 
• 7294-51-1 2,4,6-tris(4-methoxyphenyl)boroxine 
• 720-44-5 1-(4-methoxyphenyl)-1-phenylmethanol 

Downstream Products

• 40715-69-3 (1-(4-methoxyphenyl)propane-1,3-diyl)dibenzene 
• 1443367-58-5 5-(4-methoxyphenyl)-3,5-diphenyl-4,5-dihydroisoxazole 
• 1443367-84-7 3-(4-methoxyphenyl)-1,3-diphenylpropan-1-one oxime 
• 129919-78-4 trans-2-(4-Methoxyphenyl)-1,1,3-triphenylcyclopropane 
• 10035-10-6 hydrogen bromide 
• 129944-29-2 3-(4-Methoxyphenyl)-1,1,3-triphenylpropene 

Relevant articles and documents

Importance of the Reducing Agent in Direct Reductive Heck Reactions

The role of the reductant in the palladium N-heterocyclic carbene (NHC) catalyzed reductive Heck reaction and its effect on the mechanism of the reaction is reported. For the first time in this type of transformation, the palladium-NHC-catalyzed reductive

9-(Diphenylphosphino)anthracene-based phosphapalladacycle catalyzed conjugate addition of arylboronic acids to electron-deficient alkenes

9-(Diphenylphosphino)anthracene-based phosphapalladacycle catalyzed conjugate addition of arylboronic acids to electron-deficient alkenes such asα,β-unsaturated ketones, esters, nitrile and nitroalkenes gave corresponding β-arylated alkanes in good yields and achieved TON up to 700.

Electronic and Steric Tuning of an Atropisomeric Disulfoxide Ligand Motif and Its Use in the Rh(I)-Catalyzed Addition Reactions of Boronic Acids to a Wide Range of Acceptors

A novel chiral disulfoxide ligand pair bearing fluorine atoms at the 6 and 6′ position of its atropisomeric backbone, (M,S,S)- and (P,S,S)-p-Tol-6F-BIPHESO, was synthesized. Complexation to a rhodium(I) precursor gave rise to μ-Cl- and μ-OH-bridged rhodiu