134481-25-7

Basic information

• Product Name: Ethanimidoyl iodide, 2,2,2-trifluoro-N-(4-methylphenyl)-
• CAS NO: 134481-25-7
• Molecular Formula: C9H7F3IN
• Molecular Weight: 313.061
• Mol File: 134481-25-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Ethanimidoyl iodide, 2,2,2-trifluoro-N-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanimidoyl iodide, 2,2,2-trifluoro-N-(4-methylphenyl)-(134481-25-7)
• EPA Substance Registry System: Ethanimidoyl iodide, 2,2,2-trifluoro-N-(4-methylphenyl)-(134481-25-7)

Safety Data

• Hazardous Substances Data: 134481-25-7(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 126855-72-9 N-(4-methylphenyl)-2,2,2-trifluoroacetimidoyl chloride 

Downstream Products

• 145176-40-5 p-Tolyl-[(E)-1-trifluoromethyl-non-2-en-(E)-ylidene]-amine 
• 134481-16-6 [(E)-3-Benzenesulfonyl-1-trifluoromethyl-prop-2-en-(E)-ylidene]-p-tolyl-amine 
• 144008-19-5 3,3,3-Trifluoro-2-[(E)-p-tolylimino]-propionic acid butyl ester 
• 144008-24-2 2,2,2-Trifluoro-N-p-tolyl-acetimidic acid phenyl ester 
• 1373127-99-1 (E)-methyl 3-(2-(2,2,2-trifluoro-1-p-tolylethylamino)benzo[b]thiophen-3-yl)acrylate 
• 1373128-05-2 4-methylphenyl-[3-(2-methylthiophenyl)-1-trifluoromethylprop-2-ynylidene]amine 
• 1111327-40-2 C₂₁H₁₄F₃N 
• 350-96-9 2,2,2-trifluoro-N-(4-methylphenyl)acetamide 
• 144008-21-9 3,3,3-Trifluoro-2-[(E)-p-tolylimino]-propionic acid benzyl ester 
• 134481-22-4 5,5,5-Trifluoro-4-[(E)-p-tolylimino]-pent-2-ynoic acid ethyl ester 
• 144008-23-1 3,3,3-Trifluoro-2-[(E)-p-tolylimino]-propionic acid 2-chloro-ethyl ester 
• 134481-21-3 p-Tolyl-[1-trifluoromethyl-hept-2-yn-(E)-ylidene]-amine 
• 144008-20-8 3,3,3-Trifluoro-2-[(E)-p-tolylimino]-propionic acid isopropyl ester 
• 134481-23-5 [3-Phenyl-1-trifluoromethyl-prop-2-yn-(E)-ylidene]-p-tolyl-amine 

Relevant articles and documents

Homologation of trifluoroacetimidoyl iodides by palladium-catalyzed carbonylation. An approach to α-amino perfluoroalkanoic acids

Homologation of trifluoroacetimidoyl iodides and the related perfluoro-compounds by palladium-catalyst under CO(1atm)-atmosphere in the presence of alcohols gives α-imino perfluoroalkanoates which are transformed to α-amino perfluoroalkanoic acids.