350-98-1

Basic information

• Product Name: Benzamide, N-[4-(trifluoromethyl)phenyl]-
• CAS NO: 350-98-1
• Molecular Formula: C14H10F3NO
• Molecular Weight: 265.235
• Mol File: 350-98-1.mol
• Article Data: 53

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[4-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[4-(trifluoromethyl)phenyl]-(350-98-1)
• EPA Substance Registry System: Benzamide, N-[4-(trifluoromethyl)phenyl]-(350-98-1)

Safety Data

• Hazardous Substances Data: 350-98-1(Hazardous Substances Data)

Upstream product

• 455-14-1 4-trifluoromethylphenylamine 
• 98-88-4 benzoyl chloride 
• 4771-80-6 1,2,5,6-tetrahydrobenzoic acid 
• 591-50-4 iodobenzene 
• 67-66-3 chloroform 
• 100-52-7 benzaldehyde 
• 139032-23-8 1-isocyano-4-(trifluoromethyl)benzene 
• 1864-94-4 phenyl formate 
• 455-13-0 4-Iodobenzotrifluoride 
• 100-47-0 benzonitrile 
• 402-43-7 p-trifluoromethylphenyl bromide 
• 55-21-0 benzamide 
• 128796-39-4 4-trifluoromethylphenylboronic acid 
• 38117-54-3 cyclopentadienyl iron(II) dicarbonyl dimer 

Downstream Products

• 7472-54-0 N-(p-methoxyphenyl)benzamide 
• 22864-65-9 N-methyl-4-(trifluoromethyl)aniline 
• 100-51-6 benzyl alcohol 
• 343617-78-7 N-(4-(trifluoromethyl)phenyl)benzothioamide 
• 1620817-48-2 2-phenyl-6-(trifluoromethyl)benzo[d]oxazole 
• 1446786-09-9 2,4-diphenyl-6-(trifluoromethyl)quinazoline 
• 1609460-36-7 N-benzyl-N′-(4-(trifluoromethyl)phenyl)benzimidamide 
• 1305221-98-0 N-phenyl-N-4-trifluoromethylphenylbenzamide 
• 188122-52-3 (E)-2-hexenyl N-[4-(trifluoromethyl)phenyl]benzimidate 
• 206360-82-9 N-(4-Trifluoromethyl-phenyl)-benzimidic acid (Z)-hex-2-enyl ester 
• 206360-81-8 N-(4-Trifluoromethyl-phenyl)-benzimidic acid (E)-4-methyl-pent-2-enyl ester 
• 206360-79-4 N-(4-Trifluoromethyl-phenyl)-benzimidic acid (E)-hex-2-enyl ester 
• 425366-09-2 N-(4-trifluoromethyl-phenyl)-benzimidic acid 4-cyano-phenyl ester 
• 425366-22-9 phenylmethylidyne-(4-trifluoromethyl-phenyl)-ammonium 

Relevant articles and documents

Iron-catalyzed cross-coupling of N?methoxy amides and arylboronic acids for the synthesis of N-aryl amides

An efficient iron-catalyzed synthesis of N-aryl amides from N?methoxy amides and arylboronic acids is developed. FeCl3 is used as the sole catalyst for the cross-coupling reaction between N?methoxy amides and arylboronic acids without any other

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.