112476-37-6

Basic information

• Product Name: benzenetellurinyl trifluoroacetate
• Synonyms: benzenetellurinyl trifluoroacetate
• CAS NO: 112476-37-6
• Molecular Weight: 333.721
• Mol File: 112476-37-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: benzenetellurinyl trifluoroacetate(CAS DataBase Reference)
• NIST Chemistry Reference: benzenetellurinyl trifluoroacetate(112476-37-6)
• EPA Substance Registry System: benzenetellurinyl trifluoroacetate(112476-37-6)

Safety Data

• Hazardous Substances Data: 112476-37-6(Hazardous Substances Data)

Upstream product

• 32294-60-3 diphenyl ditelluride 
• 2712-78-9 bis-[(trifluoroacetoxy)iodo]benzene 
• 94971-86-5 benzenetellurinic acid anhydride 
• 407-25-0 trifluoroacetic anhydride 
• 76-05-1 trifluoroacetic acid 

Downstream Products

• 589-09-3 N-allyl-N-phenylamine 
• 112476-19-4 ethyl <2-(phenyltelluro)cyclopentyl>carbamate 
• 112476-15-0 ethyl <3-phenyl-2-(phenyltelluro)propyl>carbamate 
• 112476-14-9 ethyl <2-phenyl-1-<(phenyltelluro)methyl>ethyl>carbamate 
• 112476-39-8 ethyl <1-<(phenyltelluro)methyl>pentyl>carbamate 
• 112476-40-1 ethyl <2-(phenyltelluro)hexyl>carbamate 
• 112476-13-8 ethyl <2-(phenyltelluro)hexadecyl>carbamate 
• 112476-41-2 ethyl <1-<(phenyltelluro)methyl>pentadecyl>carbamate 
• 112476-21-8 ethyl <2-(phenyltelluro)cycloheptyl>carbamate 
• 112476-16-1 ethyl <2-phenoxy-1-<(phenyltelluro)methyl>ethyl>carbamate 
• 112476-17-2 ethyl <3-phenoxy-2-(phenyltelluro)propyl>carbamate 
• 112476-22-9 ethyl <2-(phenyltelluro)indanyl>carbamate 
• 112476-20-7 ethyl <2-(phenyltelluro)cyclohexyl>carbamate 
• 112476-18-3 ethyl <1-methyl-1-phenyl-2-(phenyltelluro)ethyl>carbamate 

Relevant articles and documents

Hypervalent iodine in synthesis: XVII. Actin of phenyliodine (III) dicarboxylates on diaryl ditellurides: A new and facile method for the preparation of arenetellurinic mixed anhydrides and arenetellurinic anhydrides

A new and facile method for the preparation of arenetelurinic mixed anhydrides is described from diaryl ditellurides and phenyliodine (III) dicarboxylates. Hydrolysis of the arenetellurinic mixed anhydrides gives arenetellurinic anhydrides and a one-pot p

TRANSFORMATION OF ALLYLSILANES INTO ALLYLAMINES VIA PHENYLTELLURINYLATION

Allylsilanes were treated with benzenetellurinyl trifluoracetate below room temperature followed by amines at 65 deg.C in 1,2-dichloroethane in the presence of boron trifluoride etherate, readily giving allylamines.

Aminotellurinylation of Olefins with Benzenetellurinyl Acetate and Ethyl Carbamate

Benzenetellurinyl acetate or trifluoroacetate in combination with ethyl carbamate effected aminotellurinylation of olefins in chloroform under reflux in the presence of boron trifluoride etherate to give ethyl carbamates in high yi