606145-74-8

Basic information

• Product Name: N-(2-cyano-4,5-dimethoxyphenyl)benzonitrile
• Synonyms: N-(2-cyano-4,5-dimethoxyphenyl)benzonitrile
• CAS NO: 606145-74-8
• Molecular Weight: 282.299
• Mol File: 606145-74-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(2-cyano-4,5-dimethoxyphenyl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-cyano-4,5-dimethoxyphenyl)benzonitrile(606145-74-8)
• EPA Substance Registry System: N-(2-cyano-4,5-dimethoxyphenyl)benzonitrile(606145-74-8)

Safety Data

• Hazardous Substances Data: 606145-74-8(Hazardous Substances Data)

Upstream product

• 26961-27-3 2-amino-4,5-dimethoxybenzonitrile 
• 98-88-4 benzoyl chloride 
• 108-86-1 bromobenzene 
• 13939-06-5 molybdenum hexacarbonyl 

Downstream Products

• 1227807-99-9 C₁₉H₁₈N₂O₂ 
• 371945-74-3 6,7-dimethoxy-2-phenylquinazolin-4(3Η)-one 
• 1229610-00-7 6,7-dimethoxy-2,4-diphenylquinazoline 

Relevant articles and documents

Pd-Catalyzed tandem reaction of N-(2-cyanoaryl)benzamides with arylboronic acids: synthesis of quinazolines

The synthesis of 2,4-disubstituted quinazolines by a palladium-catalyzed reaction of arylboronic acids with N-(2-cyanoaryl)benzamides has been developed with moderate to excellent yields. The method shows good functional group tolerance. In particular, ha

Palladium-catalyzed carbonylative synthesis of N-(2-cyanoaryl)benzamides and sequential synthesis of quinazolinones

A convenient procedure for the synthesis of N-(2-cyanoaryl)benzamides has been developed. Using aryl bromides and 2-aminobenzonitriles as the substrates, Mo(CO)6 as the CO source, the desired amides were produced in good yields. Quinazolinones