177838-10-7

Basic information

• Product Name: Benzenamine, 4-methoxy-N-(2,2,2-trifluoroethylidene)-, (E)-
• CAS NO: 177838-10-7
• Molecular Formula: C9H8F3NO
• Molecular Weight: 203.164
• Mol File: 177838-10-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-methoxy-N-(2,2,2-trifluoroethylidene)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-methoxy-N-(2,2,2-trifluoroethylidene)-, (E)-(177838-10-7)
• EPA Substance Registry System: Benzenamine, 4-methoxy-N-(2,2,2-trifluoroethylidene)-, (E)-(177838-10-7)

Safety Data

• Hazardous Substances Data: 177838-10-7(Hazardous Substances Data)

Upstream product

• 75999-66-5 (Z)-2,2,2-trifluoro-N-(4-methoxyphenyl)acetimidoyl chloride 
• 104-94-9 4-methoxy-aniline 
• 421-53-4 2,2,2-trifluoro-1,1-ethanediol 
• 433-27-2 ethyl trifluoroacetaldehyde hemiacetal 
• 75-90-1 2,2,2-Trifluoroacetaldehyde 

Downstream Products

• 850786-05-9 (4-methoxyphenyl)-(3-phenyl-1-trifluoromethyl-prop-2-ynyl)-amine 
• 62158-95-6 4-methoxy-N-(2,2,2-trifluoroethyl)aniline 
• 1020206-56-7 C₁₂H₁₆F₃NO 
• 1020206-58-9 C₁₄H₂₀F₃NO 
• 1020206-60-3 C₁₁H₁₄F₃NO 
• 1020206-62-5 C₁₃H₁₈F₃NO 
• 592537-94-5 N-(4-methoxyphenyl)-N-[1-(trifluoromethyl)-3-butenyl]amine 

Relevant articles and documents

Facile preparation of polyfluoroalkylated aldimines from polyfluoroalkanoic acids

Polyfluoroalkylated aldimines were prepared by reducing polyfluoroalkyl imidoyl chlorides, which are readily available from polyfluoroalkanoic acids, with LTBA (lithium tri-tert-butoxyaluminum hydride). Georg Thieme Verlag Stuttgart.

Chiral sulfoxide controlled asymmetric additions to C-N double bond. An efficient approach to stereochemically defined α-fluoroalkyl amino compounds

This paper presents a full account of studies into the asymmetric addition reactions between α-lithium derivatives of enantiomerically pure methyl and benzyl p-tolyl sulfoxides and the N-(p-methoxyphenyl)aldimines, bearing trifluoromethyl, pentafluoroethy

Stereoselective additions of α-lithiated alkyl-p-tolylsulfoxides to N-PMP(fluoroalkyl)aldimines. An efficient approach to enantiomerically pure fluoro amino compounds

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