94837-99-7

Upstream product

• 354-58-5 1,1,1-Trichloro-2,2,2-trifluoroethane 
• 555-16-8 4-nitrobenzaldehdye 
• 103654-96-2 1-(α,α-dichloro-β,β,β-trifluoroethyl)benzylalcohol 
• 34091-69-5 (2-chloro-3,3,3-trifluoroprop-1-en-1-yl)benzene 

Downstream Products

• 1983-22-8 1-nitro-4-(3,3,3-trifluoroprop-1-yn-1-yl)benzene 
• 1148050-15-0 1-[(1Z)-2-tert-butoxy-3,3,3-trifluoroprop-1-enyl]-4-nitrobenzene 
• 1214989-11-3 (Z)-3,3,3-trifluoro-1-(4-nitrophenyl)-N-(1-phenylethyl)prop-1-en-2-amine 
• 1214989-12-4 N-[1,1,1-trifluoro-3-(4-nitrophenyl)propan-2-ylidene]-1-phenylethanamine 
• 1214989-14-6 N-[1,1,1-trifluoro-3-(4-nitrophenyl)propan-2-ylidene]-1,1-dimethoxypropan-2-amine 
• 1214989-13-5 (Z)-3,3,3-trifluoro-N-(1,1-dimethoxypropan-2-yl)-1-(4-nitrophenyl)prop-1-en-2-amine 
• 1214989-10-2 N-[1,1,1-trifluoro-3-(4-nitrophenyl)propan-2-ylidene]-2-phenylethanamine 
• 1214989-09-9 (Z)-3,3,3-trifluoro-1-(4-nitrophenyl)-N-phenethylprop-1-en-2-amine 
• 1214989-08-8 N-[1,1,1-trifluoro-3-(4-nitrophenyl)propan-2-ylidene]propan-2-amine 
• 1214989-07-7 (Z)-3,3,3-trifluoro-N-isopropyl-1-(4-nitrophenyl)prop-1-en-2-amine 
• 1214989-06-6 N-[1,1,1-trifluoro-3-(4-nitrophenyl)propan-2-ylidene]methanamine 
• 1239902-30-7 2-(4-nitrobenzyl)-4-ethyl-2-(trifluoromethyl)oxazolidine 
• 1239902-28-3 2-(4-nitrobenzyl)-2-(trifluoromethyl)-1,3-oxazolidine 
• 1239902-18-1 2-(4-nitrobenzyl)-2-(trifluoromethyl)imidazolidine 

Relevant academic research and scientific papers

New approach to the synthesis of trifluoromethylvinyl sulfides

Nucleophilic substitution reaction of halogen atom in β-chloro-and β-bromo-β-trifluoromethylstyrenes by thiolates was studied. Stereo-and regioselectivity of the reaction with respect to the electronic and sterical properties of substituents in the aromat

Synthesis of 1-Aryl-3,3,3-trifluoro-1-propynes and 3,5-Diaryl-4-trifluoromethylisoxazoles

Diaryl-substituted trifluoromethylisoxazoles 5a-i, 6a-c, and 6e-i are synthesized from aromatic nitrile oxides and various substituted 1-aryl-3,3,3-trifluoro-1-propynes.

Synthesis of N-Acetyl-1,2-didehydrodopamine. A Key Intermediate Involved in Sclerotization of Insect Cuticule

The synthesis of N-acetyl-1,2-didehydrodopamine (6; N-acetyl-3,4-dihydroxystyrylamine) was accomplished by demethylation of N-acetyl-3,4-dimethoxystyrylamine (5), formed by sequential treatment of 3,4-dimethoxycinnamic acid (1) with thionyl chloride, sodi