114046-25-2

Basic information

• Product Name: Benzonitrile, 4-[[(4-methoxyphenyl)imino]methyl]-, (E)-
• CAS NO: 114046-25-2
• Molecular Formula: C15H12N2O
• Molecular Weight: 236.273
• Mol File: 114046-25-2.mol
• Article Data: 34

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 4-[[(4-methoxyphenyl)imino]methyl]-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 4-[[(4-methoxyphenyl)imino]methyl]-, (E)-(114046-25-2)
• EPA Substance Registry System: Benzonitrile, 4-[[(4-methoxyphenyl)imino]methyl]-, (E)-(114046-25-2)

Safety Data

• Hazardous Substances Data: 114046-25-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 62-53-3 aniline 
• 105-07-7 4-cyanobenzaldehyde 
• 136827-57-1 4-[(E)-2-(4-hydroxyphenyl)ethenyl]benzonitrile 
• 2101-87-3 p-methoxy-phenylazide 
• 104-94-9 4-methoxy-aniline 
• 100-17-4 para-methoxynitrobenzene 
• 874-89-5 4-Cyanobenzyl alcohol 
• 3435-51-6 4-ethenylbenzonitrile 
• 5416-93-3 4-Methoxyphenyl isocyanate 

Downstream Products

• 1039451-65-4 (2E,5S)-ethyl 5-(4-methoxyphenylamino)-5-(4-cyanophenyl)-pent-2-enoate 
• 959290-96-1 4-(6-methoxyquinolin-2-yl)benzonitrile 
• 1245136-10-0 2-(4-cyanophenyl)-1-(4-methoxyphenyl)-2,3-dihydropyridin-4(1H)-one 
• 1326705-12-7 (1S,2S)-N-(4-methoxyphenyl)-1-(4-cyanophenyl)-2-(methylsulfenyl)-2-{2-[(S)-p-tolylsulfinyl]phenyl}ethylamine 
• 1326705-23-0 (1S,2S)-N-(4-methoxyphenyl)-1-(4-cyanophenyl)-2-(methylsulfenyl)-2-phenylethylamine 

Relevant articles and documents

Enantioselective direct aza hetero-Diels-Alder reaction catalyzed by chiral Bronsted acids

(Chemical Equation Presented) The first chiral Bronsted acid-catalyzed asymmetric direct aza hetero-Diels-Alder reaction has been described. The phosphoric acids, prepared from binol and H8-binol derivatives, have shown catalytic ability for th

Nanomagnetic catalysis (Fe3O4@S–TiO2): a novel magnetically nano catalyst for the synthesis of new highly substituted tetrahydropyridine derivatives under solvent-free conditions

A novel nanomagnetic catalyst (Fe3O4@S–TiO2) was prepared by the hydrothermal method. At the first, Fe3O4 nanoparticles were synthesized, then iron oxide nanoparticles (IONPs) were dispersed in ethano

Carbon monoxide-driven osmium catalyzed reductive amination harvesting WGSR power

Herein, we present the first example of Os-catalyzed efficient reductive amination under water-gas shift reaction conditions. The developed catalytic systems are formedin situin aqueous solutions, employ as small as 0.0625 mol% osmium and are capable of delivering reductive amination products for a broad range of aliphatic and aromatic carbonyl compounds and amines. The scope of the reaction, active catalytic systems, possible limitations of the method and DFT-supported mechanistic considerations are discussed in detail in the manuscript.

Enantioselective Direct anti-Selective Mannich-type Reactions Catalyzed by 3-Pyrrolidinecarboxylic Acid in the Presence of Potassium Carbonate: Addition of Potassium Carbonate Improves Enantioselectivities

Mannich-type reactions of cyclohexanone and related six-membered-ring ketones with N-p-methoxyphenyl-protected imines of arylaldehydes catalyzed by 3-pyrrolidinecarboxylic acid in the presence of K2CO3 that afford anti-isomers of the Mannich products with