865541-03-3

Basic information

• Product Name: (R)-3-(4-methoxyphenyl)-1-phenylbutan-1-one
• Synonyms: (R)-3-(4-methoxyphenyl)-1-phenylbutan-1-one
• CAS NO: 865541-03-3
• Molecular Weight: 254.329
• Mol File: 865541-03-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (R)-3-(4-methoxyphenyl)-1-phenylbutan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-(4-methoxyphenyl)-1-phenylbutan-1-one(865541-03-3)
• EPA Substance Registry System: (R)-3-(4-methoxyphenyl)-1-phenylbutan-1-one(865541-03-3)

Safety Data

• Hazardous Substances Data: 865541-03-3(Hazardous Substances Data)

Upstream product

• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 495-41-0 1-phenylbut-2-en-1-one 
• 5720-07-0 4-methoxyphenylboronic acid 
• 107805-20-9 3ξ-(4-methoxy-phenyl)-2-methyl-1-phenyl-propenone 
• 1125576-35-3 (R)-N-(1-(4-methoxyphenyl)ethyl)-4-methyl-benzenesulfonamide 
• 614-20-0 3-oxo-3-phenylpropionic acid 
• 70-11-1 α-bromoacetophenone 
• 50640-96-5 (R,S)-NN-dimethyl-1-p-methoxyphenylethylamine 
• 87258-60-4 2-dimethylamino-3-p-methoxyphenyl-1-phenylbutan-1-one 
• 1376710-73-4 (E)-N-methoxy-3-(4-methoxyphenyl)-N-methylbut-2-enamide 
• 99142-77-5 methyl (E)-3-(3-methoxyphenyl)-3-methylacrylate 

Relevant articles and documents

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

Diastereoselective Radical Oxidative C-H Aminations toward Chiral Atropoisomeric (P, N) Ligand Precursors

A new class of chiral atropoisomeric (P, N) ligand precursors has been obtained with excellent diastereoselectivities and high yields through diastereoselective metal-free intramolecular radical oxidative C-H amination with chiral phosphamide as the auxil

Catalytic decarboxylative alkylation of β-keto acids with sulfonamides via the cleavage of carbon-nitrogen and carbon-carbon bonds

An efficient decarboxylative alkylation reaction of β-keto acids with N-benzylic or N-allylic sulfonamides has been developed, for the first time, through sequential cleavage of carbon-nitrogen and carbon-carbon bonds in the presence of 10 mol% of FeCl3.