2002-95-1

Upstream product

• 791-50-4 2,2,4,4-Tetrakis(trifluoromethyl)-1,3-dithietane 
• 62-53-3 aniline 
• 421-50-1 1,1,1-trifluoro-2-propanone 
• 26350-10-7 diphenyl phenylphosphoramidite 
• 291752-78-8 C₃₃H₃₂F₁₂NO₂P 
• 684-16-2 Hexafluoroacetone 
• 2325-27-1 N-phenyltriphenyliminophosphorane 
• 382-21-8 perfluoroisobutylene 
• 586-96-9 Nitrosobenzene 
• 103-71-9 phenyl isocyanate 
• 41399-75-1 2,2-diphenoxy-3-phenyl-4,4-bis-trifluoromethyl-2-(2,2,2-trifluoro-1-trifluoromethyl-ethoxy)-2λ⁵-[1,3,2]oxazaphosphetidine 

Downstream Products

• 50849-65-5 2-Methoxy-2-phenylaminohexafluorpropan 
• 1736-36-3 2-Aethoxy-2-phenylamino-hexafluorpropan 
• 1736-12-5 N-(1,1,1,3,3,3-hexafluoropropyl)aniline 
• 1540-86-9 (1-anilino-2,2,2-trifluoro-1-trifluoromethyl)ethylhydrazine 
• 1737-14-0 2-Amino-2-anilino-1.1.1.3.3.3-hexafluor-propan 
• 2342-51-0 2-Anilino-2-isobutylamino-1.1.1.3.3.3-hexafluor-propan 
• 50849-87-1 3-phenyl-2,2-bis-trifluoromethyl-thiazolidin-4-one 
• 1540-95-0 2-Anilino-1.1.1.3.3.3-hexafluor-2-dimethylamino-propan 
• 1995-79-5 2-Anilino-2-benzylamino-1,1,1,3,3,3-hexafluor-propen 
• 50849-80-4 2-Aethylthio-2-phenylaminohexafluorpropan 
• 104765-34-6 1-phenyl-2,2-difluoro-3,3-bis(trifluoromethyl)aziridine 
• 85290-62-6 2-phenylamino-1,1,3,3,3-pentafluoropropene 
• 128038-40-4 N-hexafluoro-tert-butylaniline 
• 334866-55-6 [1-({2-[1-(tert-butyl-dimethyl-silanyloxy)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenylselanyl}-phenyl-methyl)-2,2,2-trifluoro-1-trifluoromethyl-ethyl]-phenyl-amine 

Relevant academic research and scientific papers

Formylation of fluoroalkyl imines through visible-light-enabled H-atom transfer catalysis: Access to fluorinated α-amino aldehydes

A visible-light-enabled catalytic formylation of fluoroalkyl imines is developed. With readily accessible starting materials and organocatalysts, this method provides a general approach to masked fluoroalkyl amino aldehydes. A synergistic catalytic effect

Synthesis, structure, and thermolysis of pentacoordinate 1,3,2λ5- oxazaphosphetidines: The intermediates of aza-Wittig reactions

1,3,2λ5-Oxazaphosphetidines bearing the Martin ligand were synthesized by the reaction of the corresponding iminophosphorane and carbonyl compounds and characterized by X-ray crystallographic analysis. Thermolysis of the oxazaphosphetidine gave

High-pressure 19F NMR study of the degenerate isomerization of hexafluoroacetone anils. Evidence for the existence of two different inversion transition states

Solvent, temperature, and pressure effects on the rate of the degenerate isomerization of hexafluoroacetone anils were studied by 19F NMR. The results unequivocally demonstrated that the mechanism is not rotation about the carbon-nitrogen bond