106376-18-5

Basic information

• Product Name: N-phenyl-3-(trifluoromethyl)benzamide
• Synonyms: N-phenyl-3-(trifluoromethyl)benzamide
• CAS NO: 106376-18-5
• Molecular Formula: C₁₄H₁₀F₃NO
• Molecular Weight: 265.2305096
• Mol File: 106376-18-5.mol
• Article Data: 14

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-phenyl-3-(trifluoromethyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenyl-3-(trifluoromethyl)benzamide(106376-18-5)
• EPA Substance Registry System: N-phenyl-3-(trifluoromethyl)benzamide(106376-18-5)

Safety Data

• Hazardous Substances Data: 106376-18-5(Hazardous Substances Data)

Upstream product

• 2251-65-2 3-(Trifluoromethyl)benzoyl chloride 
• 62-53-3 aniline 
• 425366-16-1 phenyl-(3-trifluoromethyl-phenylmethylidyne)-ammonium 
• 425366-00-3 N-phenyl-3-trifluoromethyl-benzimidic acid 4-cyano-phenyl ester 
• 591-50-4 iodobenzene 
• 1801-10-1 3-trifluoromethylbenzamide 
• 368-77-4 3-trifluoromethylbenzonitrile 
• 98-80-6 phenylboronic acid 
• 58710-61-5 phenyl 3-(trifluoromethyl)benzoate 
• 201230-82-2 carbon monoxide 
• 401-81-0 m-trifluoromethylphenyl iodide 
• 76783-59-0 ethyl 3-(trifluoromethyl)benzoate 
• 98-95-3 nitrobenzene 
• 723252-38-8 C₁₄H₉ClF₃NO 

Downstream Products

• 350487-59-1 N'-methoxy-N-phenyl-3-(trifluoromethyl)benzimidamide 
• 1609460-47-0 1-benzyl-2-(3-(trifluoromethyl)phenyl)-1H-benzo[d]imidazole 
• 1609460-29-8 N-benzyl-N'-phenyl-3-(trifluoromethyl)benzimidamide 
• 1372890-84-0 4-phenyl-2-(3-(trifluoromethyl)phenyl)quinazoline 
• 425366-00-3 N-phenyl-3-trifluoromethyl-benzimidic acid 4-cyano-phenyl ester 
• 425366-16-1 phenyl-(3-trifluoromethyl-phenylmethylidyne)-ammonium 

Relevant articles and documents

Role of intermolecular interactions involving organic fluorine in trifluoromethylated benzanilides

Trifluoromethylated benzanilides, containing C(sp3)-F bonds, have been synthesized and their crystal and molecular structures have been investigated to highlight the significance of weak intermolecular interactions associated with the presence

Visible-Light-Promoted Iron-Catalyzed N-Arylation of Dioxazolones with Arylboronic Acids

A visible-light-promoted and simple iron salt-catalyzed N-arylation was achieved efficiently under external photosensitizer-free conditions. Arylboronic acids and bench-stable dioxazolones were used for this cross-coupling reaction. This reaction features high reactivity, wide substrate scope, good functional group tolerance, simple operation procedure, and mild reaction conditions. Preliminary mechanistic investigations were conducted to support a radical pathway. This method may contribute to shift the paradigm of iron-catalyzed C-N bond construction and nitrene transfer chemistry.

Exploration of Cu-catalyzed regioselective hydrodehalogenation of o-haloanilides using EtOH as hydrogen source

In present work, we have explored a Cu(acac)2/vasicine-catalyzed regioselective hydrodehalogenation methodology of o-haloanilides using EtOH as hydrogen source and solvent. The catalytic system could selectively dehalogenate 2-Br and 2-I, and features regioselective, efficient and functional group tolerance.