51431-52-8

Basic information

• Product Name: Benzene, 1-methoxy-4-(2-nitro-1-phenylethyl)-
• CAS NO: 51431-52-8
• Molecular Formula: C15H15NO3
• Molecular Weight: 257.289
• Mol File: 51431-52-8.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzene, 1-methoxy-4-(2-nitro-1-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-methoxy-4-(2-nitro-1-phenylethyl)-(51431-52-8)
• EPA Substance Registry System: Benzene, 1-methoxy-4-(2-nitro-1-phenylethyl)-(51431-52-8)

Safety Data

• Hazardous Substances Data: 51431-52-8(Hazardous Substances Data)

Upstream product

• 102-96-5 (2-nitroethenyl)benzene 
• 100-66-3 methoxybenzene 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 
• 98-80-6 phenylboronic acid 
• 3179-10-0 (E)-1-methoxy-4-(2-nitrovinyl)benzene 
• 5720-07-0 4-methoxyphenylboronic acid 
• 696-62-8 para-iodoanisole 
• 591-51-5 phenyllithium 
• 143-66-8 sodium tetraphenyl borate 
• 5153-67-3 nitrostyrene 
• 21130-91-6 triethoxy(4-methoxyphenyl)silane 
• 595-90-4 tetraphenyltin(IV) 

Downstream Products

• 4578-79-4 2-(4-methoxyphenyl)-2-phenylacetonitrile 
• 51431-54-0 2-(p-methoxyphenyl)-2-phenylethylamine 

Relevant articles and documents

A novel catalytic activity of bismuth(III) salts in palladium(II)-catalyzed atom economical Michael-type hydroarylation of nitroalkenes with aryltin compounds

A novel catalytic effect of bismuth(III) salts such as BiCl3, Bi2O3, and Bi(NO3)3·5H2O has been disclosed in new palladium(II)-catalyzed Michael-type hydroarylation of nitroalkenes with aryltin compounds. The reaction is atom economical in the tin compounds and slightly fewer than four aryl groups of tetraaryltins can be transferred to the products.

Multifunctional isoquinoline-oxazoline ligands of chemical and biological importance

Multifunctional isoquinoline-oxazolines (MIQOXs) were conceived and synthesized from commercially available chiral amino acids. The multifunctional role of MIQOXs was demonstrated by Pd-catalyzed highly enantioselective addition of arylboronic acids to nitrostyrenes, and by the discovery of novel antifungal candidates.

Stable and Reusable Palladium Nanoparticles-Catalyzed Conjugate Addition of Aryl Iodides to Enones: Route to Reductive Heck Products

An efficient, binaphthyl-backbone-stabilized palladium nanoparticles (Pd-BNP) catalyst for the 1,4-addition of aryl halides to enones has been developed. The scope of the reaction has been studied with various substituted and sterically hindered aryl hali