1429616-70-5

Basic information

• Product Name: 4-(N’-benzyl-N’-(2,2-diethoxyethyl)amino)benzonitrile
• Synonyms: 4-(N’-benzyl-N’-(2,2-diethoxyethyl)amino)benzonitrile
• CAS NO: 1429616-70-5
• Molecular Weight: 324.423
• Mol File: 1429616-70-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(N’-benzyl-N’-(2,2-diethoxyethyl)amino)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N’-benzyl-N’-(2,2-diethoxyethyl)amino)benzonitrile(1429616-70-5)
• EPA Substance Registry System: 4-(N’-benzyl-N’-(2,2-diethoxyethyl)amino)benzonitrile(1429616-70-5)

Safety Data

• Hazardous Substances Data: 1429616-70-5(Hazardous Substances Data)

Upstream product

• 160133-46-0 C₁₃H₁₈N₂O₂ 
• 100-39-0 benzyl bromide 

Downstream Products

• 80531-13-1 1-benzyl-1H-indole-5-carbonitrile 

Relevant articles and documents

General and efficient synthesis of 2,3-unsubstituted indoles catalyzed by acidic mesoporous molecular sieves

A general and efficient method for the synthesis of 2,3-unsubstituted indoles has been established by the intramolecular cyclization of N-benzyl 2-anilinoacetals. Acidic mesoporous molecular sieve (MCM-41-SO3H) has shown excellent catalytic activity on this transformation, and the 2,3-unsubstituted indoles bearing 7-substituent or strong electron-withdrawing substituents also could be achieved by this protocol. Moreover, the heterogeneous catalyst, MCM-41-SO3H, could be conveniently recovered and reused without obvious loss of the catalytic activity. This work will provide an economic and environmental-benign method for the construction of various indole derivatives.