129083-39-2

Upstream product

• 402-43-7 p-trifluoromethylphenyl bromide 

Downstream Products

• 185421-11-8 2-hydroxybutyl 4-(trifluoromethyl)phenyl telluride 
• 174277-14-6 2-hydroxy-5-hexenyl 4-(trifluoromethyl)phenyl telluride 
• 185421-13-0 2-hydroxy-2-phenylethyl 4-(trifluoromethyl)phenyl telluride 
• 185421-19-6 3-(benzyloxy)-2-hydroxypropyl 4-(trifluoromethyl)phenyl telluride 
• 185421-18-5 2-hydroxy-3-phenoxypropyl 4-(trifluoromethyl)phenyl telluride 
• 743420-47-5 2-hydroxy-3-phenylpropyl 4-(trifluoromethyl)phenyl telluride 
• 743420-52-2 2-allyloxy-3-phenylpropyl 4-(trifluoromethyl)phenyl telluride 
• 185421-23-2 2-(allyloxy)butyl 4-(trifluoromethyl)phenyl telluride 
• 185421-28-7 2,3-bis(allyloxy)propyl 4-(trifluoromethyl)phenyl telluride 
• 174277-12-4 2-(2-propynyloxy)-5-hexenyl 4-(trifluoromethyl)phenyl telluride 
• 185421-37-8 3-(allyloxy)-2-(2-propynyloxy)propyl 4-(trifluoromethyl)phenyl telluride 
• 185421-25-4 2-(allyloxy)-2-phenylethyl 4-(trifluoromethyl)phenyl telluride 
• 185421-29-8 2-(allyloxy)-3-phenoxypropyl 4-(trifluoromethyl)phenyl telluride 

Relevant academic research and scientific papers

Improved preparation of diaryl ditellurides

Diaryl ditellurides have been synthesized from aryl bromides via lithiation, tellurium insertion, and ferricyanide oxidation of the resulting lithium arenetellurolates.

Modulating Chalcogen Bonding and Halogen Bonding Sigma-Hole Donor Atom Potency and Selectivity for Halide Anion Recognition

A series of acyclic anion receptors containing chalcogen bond (ChB) and halogen bond (XB) donors integrated into a neutral 3,5-bis-triazole pyridine scaffold are described, in which systematic variation of the electronic-withdrawing nature of the aryl sub