17102-85-1

Basic information

• Product Name: N-[(benzoylamino)(4-methoxyphenyl)methyl]benzamide
• Synonyms: N-[(benzoylamino)(4-methoxyphenyl)methyl]benzamide;N,N'-[(4-methoxyphenyl)methanediyl]dibenzamide
• CAS NO: 17102-85-1
• Molecular Formula: C₂₂H₂₀N₂O₃
• Molecular Weight: 360.41
• Mol File: 17102-85-1.mol
• Article Data: 21

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-[(benzoylamino)(4-methoxyphenyl)methyl]benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(benzoylamino)(4-methoxyphenyl)methyl]benzamide(17102-85-1)
• EPA Substance Registry System: N-[(benzoylamino)(4-methoxyphenyl)methyl]benzamide(17102-85-1)

Safety Data

• Hazardous Substances Data: 17102-85-1(Hazardous Substances Data)

Upstream product

• 55-21-0 benzamide 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-47-0 benzonitrile 
• 825-60-5 benzimidic acid ethyl ester 
• 105-13-5 4-Methoxybenzyl alcohol 
• 60-35-5 acetamide 
• 25408-75-7 N,N'-dibenzoylsulfur diimide 
• 288-32-4 1H-imidazole 
• 40891-01-8 4-(dimorpholinomethyl)-1-methoxybenzene 

Downstream Products

• 10374-25-1 N-benzoyl-1-methoxy-1-(p-methoxyphenyl)-methylamine 

Relevant articles and documents

Surface modified novel magnetically tuned halloysite functionalized sulfonic acid: synthesis, characterization and catalytic activity

This work presents preparation of a surface modified magnetically tuned solid acid where thiol groups were grafted on magnetic halloysite, followed by oxidation of thiol groups to sulfonic acid groups. The physicochemical properties of the catalyst were a

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