351862-56-1

Basic information

• Product Name: 2-(2-(4-methoxyphenyl)ethynyl)benzonitrile
• Synonyms: 2-(2-(4-methoxyphenyl)ethynyl)benzonitrile
• CAS NO: 351862-56-1
• Molecular Weight: 233.269
• Mol File: 351862-56-1.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-(2-(4-methoxyphenyl)ethynyl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-(4-methoxyphenyl)ethynyl)benzonitrile(351862-56-1)
• EPA Substance Registry System: 2-(2-(4-methoxyphenyl)ethynyl)benzonitrile(351862-56-1)

Safety Data

• Hazardous Substances Data: 351862-56-1(Hazardous Substances Data)

Upstream product

• 696-62-8 para-iodoanisole 
• 40888-26-4 2-ethynylbenzonitrile 
• 2042-37-7 o-cyanobromobenzene 
• 768-60-5 4-methoxyphenylacetylen 
• 4387-36-4 2-iodobenzonitrile 

Downstream Products

• 934423-97-9 2-((E)-1-iodo-2-(4-methoxyphenyl)vinyl)benzonitrile 
• 29910-92-7 3-(4-methoxyphenyl)-1H-isochromen-1-one 
• 1192716-93-0 2-(5-(4-methoxyphenyl)-2H-1,2,3-triazol-4-yl)benzonitrile 
• 1192717-17-1 5-(4-methoxyphenyl)tetrazolo[5,1-a]isoquinoline 
• 1581713-38-3 methyl 1-amino-3-(4-methoxyphenyl)-2-naphthoate 
• 1403583-59-4 6-(4-methoxyphenyl)benzo[4,5]imidazo[2,1-a]isoquinoline (4e) 
• 1609162-33-5 ethyl 1-amino-3-(4-methoxyphenyl)-2-naphthoate 
• 13670-91-2 3-(4-methoxyphenyl)-2H-isoquinolin-1-one 
• 1260150-33-1 1-ethoxy-3-(4-methoxyphenyl)isoquinoline 
• 862604-48-6 CNC₆H₄CSn(C₄H₉)3CHC₆H₄OCH₃ 
• 934424-08-5 di(tert-butyl) 1-[(E)-1-(2-cyanophenyl)-2-(4-methoxyphenyl)ethenyl]-1,2-hydrazinedicarboxylate 

Relevant articles and documents

Selective synthesis of benzo[4,5]imidazo[2,1-a]isoquinolines via copper-catalyzed tandem annulation of alkynylbenzonitriles with 2-Iodoanilines

An efficient copper-catalyzed cascade cyclization reaction for selectively synthesizing a variety of benzo[4,5]imidazo[2,1-a]isoquinoline derivatives has been developed. The reaction features the formation of three different C–N bonds in sequence. In the

Lanthanide-Catalyzed Tandem Insertion of Secondary Amines with 2-Alkynylbenzonitriles: Synthesis of Aminoisoindoles

A lanthanide-catalyzed intermolecular hydroamination of 2-alkynylbenzonitriles with secondary amines has been disclosed, providing a streamlined access to a range of aminoisoindoles in moderate to excellent yields. The salient features of this reaction in

Synthesis of naphthalene amino esters and arylnaphthalene lactone lignans through tandem reactions of 2-alkynylbenzonitriles

Tandem reaction of 2-alkynylbenzonitriles with a Reformatsky reagent turned out to be a novel and efficient approach toward 1-aminonaphthalene-2- carboxylates. Interestingly, with 2-(3-hydroxyprop-1-ynyl)benzonitriles as the substrates, a more sophisticat