79157-37-2

Basic information

• Product Name: Benzene, 1,2-dimethoxy-4-(1-phenylethenyl)-
• CAS NO: 79157-37-2
• Molecular Formula: C16H16O2
• Molecular Weight: 240.302
• Mol File: 79157-37-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2-dimethoxy-4-(1-phenylethenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2-dimethoxy-4-(1-phenylethenyl)-(79157-37-2)
• EPA Substance Registry System: Benzene, 1,2-dimethoxy-4-(1-phenylethenyl)-(79157-37-2)

Safety Data

• Hazardous Substances Data: 79157-37-2(Hazardous Substances Data)

Upstream product

• 2316-26-9 3,4-dimethoxycinnamic acid 
• 71-43-2 benzene 
• 2859-78-1 4-Bromoveratrole 
• 98-86-2 acetophenone 
• 4038-14-6 3,4-dimethoxybenzophenone 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 100-42-5 styrene 
• 49639-26-1 erythro-2-(phenylsulfinyl)-1-phenyl-1-ethanol 
• 67210-34-8 1-phenyl-2-phenylsulfanyl-ethanol 
• 16222-10-9 1-phenyl-2-(phenylthio)ethanone 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 
• 79177-62-1 3-hydroxy-6,7-dimethoxy-9-phenylphenanthrene-1,4-quinone 
• 917-64-6 methyl magnesium iodide 

Downstream Products

• 77473-29-1 1,2-dimethoxy-4-(1-phenylethyl)benzene 
• 79177-62-1 3-hydroxy-6,7-dimethoxy-9-phenylphenanthrene-1,4-quinone 
• 79157-38-3 7-O-methyllatinone 

Relevant articles and documents

Regiodivergent DH or HD Addition to Alkenes: Deuterohydrogenation versus Hydrodeuterogenation

The regioselective and regiodivergent addition of H-D to a variety of 1,1-diarylalkenes was realized utilizing selectively deuterated dihydroaromatic compounds, which were generated by cobalt catalysis. The reaction was initiated by catalytic amounts of B

Metal- and Oxidant-Free Alkenyl C?H/Aromatic C?H Cross-Coupling Using Electrochemically Generated Iodosulfonium Ions

A three-step transformation consisting of 1) addition of electrochemically generated iodosulfonium ions to vinylarenes to give (1-aryl-2-iodoethoxy)sulfonium ions, 2) nucleophilic substitution by subsequently added aromatic compounds to give 1,1-diaryl-2-

Synthesis of 1,1-diarylethylenes

A facile route toward 1,1-diarylethylenes 6 has been developed in good yields via mCPBA-promoted oxidation of β-hydroxysulfides 2, BF3·OEt2-mediated Friedel-Crafts reaction of the resulting β-hydroxysulfoxides 3 with oxygenated benze