40891-10-9

Basic information

• Product Name: N,N′?(4?methylbenzylidene)bisbenzamide
• Synonyms: N,N′?(4?methylbenzylidene)bisbenzamide
• CAS NO: 40891-10-9
• Molecular Weight: 344.413
• Mol File: 40891-10-9.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: N,N′?(4?methylbenzylidene)bisbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N′?(4?methylbenzylidene)bisbenzamide(40891-10-9)
• EPA Substance Registry System: N,N′?(4?methylbenzylidene)bisbenzamide(40891-10-9)

Safety Data

• Hazardous Substances Data: 40891-10-9(Hazardous Substances Data)

Upstream product

• 589-18-4 4-Methylbenzyl alcohol 
• 55-21-0 benzamide 
• 100-47-0 benzonitrile 
• 104-87-0 4-methyl-benzaldehyde 
• 825-60-5 benzimidic acid ethyl ester 
• 34036-34-5 bis(morpholino)(4-methylphenyl)methane 

Downstream Products

• 65608-94-8 N-(p-methylbenzyl)benzamide 

Relevant articles and documents

Synthesis and characterization of a novel organic–inorganic hybrid salt and its application as a highly effectual Br?nsted–Lewis acidic catalyst for the production of N,N′-alkylidene bisamides

In this research, a novel organic–inorganic hybrid salt, namely, N1,N1,N2,N2-tetramethyl-N1,N2-bis(sulfo)ethane-1,2-diaminium tetrachloroferrate ([TMBSED][FeCl4]2) was

Benzimidates as gem-Diamidation and Amidoindolyzation Cascade Synthons with a Hydrated NiII Catalyst

We contributed a new benzimidate chemistry through moisture-insensitive NiII/NiII-FeIII combo-catalysis for a simultaneous 2-3 bond-forming gem-diamidation and amidoindolyzation cascade reaction to construct symmetrical an

The synthesis and structure of pyridine-oxadiazole iridium complexes and catalytic applications: Non-coordinating-anion-tuned selective C–N bond formation

Several novel pyridine-oxadiazole iridium complexes were synthesized and characterized through X-ray crystallography. The designed iridium complexes revealed surprisingly high catalytic activity in C–N bondformation of amides and benzyl alcohols with the assistance of non-coordinating anions. In an attempt to achieve borrowing hydrogen reactions of amides with benzyl alcohols, N,N'-(phenylmethylene)dibenzamide products were unexpectedly isolated under non-coordinating anion conditions, whereas N-benzylbenzamide products were achieved in the absence of non-coordinating anions. The mechanism explorations excluded the possibility of “silver effect” (silver-assisted or bimetallic catalysis) and revealed that the reactivity of iridium catalyst was varied by non-coordinating anions. This work provided a convenient and useful methodology that allowed the iridium complex to be a chemoselective catalyst and demonstrated the first example of non-coordinating-anion-tuned selective C–N bond formation