55136-88-4

Basic information

• Product Name: Benzene, 1,1'-[methylenebis(telluro)]bis-
• CAS NO: 55136-88-4
• Molecular Formula: C13H12Te2
• Molecular Weight: 423.438
• Mol File: 55136-88-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-[methylenebis(telluro)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-[methylenebis(telluro)]bis-(55136-88-4)
• EPA Substance Registry System: Benzene, 1,1'-[methylenebis(telluro)]bis-(55136-88-4)

Safety Data

• Hazardous Substances Data: 55136-88-4(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 75-11-6 diiodomethane 
• 591-51-5 phenyllithium 
• 14683-12-6 tellurium 
• 186581-53-3 diazomethane 
• 32294-60-3 diphenyl ditelluride 

Downstream Products

• 102-04-5 1,3-Diphenylpropanone 
• 103-79-7 1-phenyl-acetone 
• 55136-89-5 (RS)-1-phenyl-2-(phenyltellanyl)ethanol 
• 55136-93-1 2-Phenyl-1,1-bis-(phenyltelluro)ethane 
• 872-89-9 methylphenyltelluride 
• 451-40-1 phenyl benzyl ketone 
• 77953-91-4 1,1-bis(phenyltelluro)dodecane 
• 75250-42-9 n-dodecyl(phenyl)telluride 

Relevant articles and documents

Chiral Organometallic Reagents, XVI. Enantiomerization of α-Thio-, α-Seleno-, and α-Telluro-Substituted Alkyllithium Compounds; Kinetic and Mechanistic Studies

The rate of enantiomerization of the racemic α-phenylselenoalkyllithium compound 6 has been determined by dynamic NMR spectroscopy in THF.The enantiomerization rate was found to be first order with respect to monomeric 6 and to show no conspicuous sol

Synthesis of chelating ditelluroether ligands, RTeCH2CH2CH2TeR (R = Me, Ph)

RTeLi (R = Me, Ph), prepared in situ in tetrahydrofuran from RLi and Te, react at low temperatures with 1,3-dihalopropanes, X(CH2)3X (X = Cl, Br), to give high yields of RTe(CH2)3TeR. At ambient or higher temperatures these reactions yield mainly R2Te2. The RTeCH2TeR are made analogously, but 1,2-dichloroethane gave only R2Te2.