172216-91-0

Basic information

• Product Name: α,α,α-trifluoro-N-phenyl-o-acetotoluidide
• Synonyms: α,α,α-trifluoro-N-phenyl-o-acetotoluidide
• CAS NO: 172216-91-0
• Molecular Weight: 279.262
• Mol File: 172216-91-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: α,α,α-trifluoro-N-phenyl-o-acetotoluidide(CAS DataBase Reference)
• NIST Chemistry Reference: α,α,α-trifluoro-N-phenyl-o-acetotoluidide(172216-91-0)
• EPA Substance Registry System: α,α,α-trifluoro-N-phenyl-o-acetotoluidide(172216-91-0)

Safety Data

• Hazardous Substances Data: 172216-91-0(Hazardous Substances Data)

Upstream product

• 344-62-7 N-[2-(trifluoromethyl)phenyl]acetamide 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 392-83-6 o-trifluoromethylphenyl bromide 
• 103-84-4 Acetanilid 
• 108-86-1 bromobenzene 
• 172217-04-8 α,α,α-trifluoro-o-diacetotoluidide 
• 88-17-5 2-(trifluoromethyl)benzenamine 

Downstream Products

• 14925-11-2 α,α,α-trifluoro-N-phenyl-o-toluidine 
• 172216-94-3 ethyl pyruvate 2-<2-(trifluoromethyl)phenyl>phenylhydrazone 
• 172216-92-1 α,α,α-trifluoro-N-nitroso-N-phenyl-o-toluidine 
• 172216-93-2 1-<2-(trifluoromethyl)phenyl>-1-phenylhydrazine 
• 23868-11-3 ethyl 2-(phenylamino)benzoate 

Relevant articles and documents

Antiviral Compounds

Novel compounds, methods, and compositions for treating various viral infections are described. In some embodiments the novel compounds of the invention are 3-oxo-phenothiazine derivatives; more specific embodiments include 3-oxo-phenothiazine derivatives having substituents at the 1-, 7-, and 9-positions of the phenothiazine parent ring. In other embodiments, the invention provides compositions and methods for treating viral infections, especially HIV.

Synthesis of substituted coumarinyloxy triazoles and thiadiazoles and their antimicrobial activity

Hydrazides and thiosemicarbazides of substituted coumarins have been synthesised by condensing substituted carbethoxy coumarins with hydrazine hydrate and aryl isothiocyanates respectively.The thiosemicarbazides when cyclised on treatment with NaOH and conc.H2SO4 give triazoles and thiadiazoles.The synthesised compounds have been tested for their anti-microbial activity against Alternaria brassicicola, Fusarium udam, Staphylococcus gram (-ve), Lactobacilus gram (-ve).However none of them show any significant activity.

Synthesis of coumarin derivatives as possible antifungal and antibacterial agents

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