36309-69-0

Upstream product

• 35684-37-8 bis(4-methoxyphenyl)ditelluride 
• 108162-22-7 phenyl(p-methoxyphenyltelluro)acetylene 
• 76204-52-9 4-Methyl-tellurobenzoic acid Te-(4-methoxy-phenyl) ester 

Downstream Products

• 115022-75-8 C₁₂H₁₆Br₂O₂Te 
• 115022-79-2 C₁₄H₁₈Br₂O₂Te 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 63971-79-9 <4-Methoxy-phenyl>-<4-dimethylamino-phenyl>-tellurdibromid 
• 35684-37-8 bis(4-methoxyphenyl)ditelluride 
• 113345-01-0 2-<<(p-methoxyphenyl)telluro>methyl>tetrahydrofuran 
• 115075-20-2 6-(4-Methoxy-phenyltellanyl)-hexahydro-cyclopenta[b]furan 
• 63971-80-2 <4-Methoxy-phenyl>-<4-dimethylamino-phenyl>-tellurdiiodid 
• 63212-69-1 p-dimethylaminophenyl(p-methoxyphenyl)tellurium(II) 
• 108924-84-1 (4-Methoxy-phenyl)-(2,4-dihydroxy-phenyl)-tellurdibromid 
• 125689-62-5 Phenacyl-<4-methoxy-phenyl>-tellurdibromid 

Relevant academic research and scientific papers

1,1,2-Trihaloalkenes and Dimeric Acetylenes from Acetylenic Tellurium Species

Reaction of 1-telluroalk-1-ynes with bromine and iodine or with Cu(II) chloride furnishes respectively 1,1,2-trihaloalkenes and 1,4-disubstituted 1,3-diynes.

Facile Reaction of Te-Aryl Benzenecarbotelluroates, ArCOTeAr', with Methyl Iodide and Halogens

Reaction of Te-aryl benzenecarbotelluroates of the type ArCOTeAr' (Ar=phenyl p-tolyl, p-bromophenyl; Ar'=phenyl, p-methoxyphenyl) with methyl iodide was found to give symmetrical telluronium salts, (1+)I(1-) in good yields.The reactivity of one of these benzene carbotelluroates towards halogens was also examined.