20334-43-4

Basic information

• Product Name: dimethyl ditelluride
• Synonyms: Dimethyl ditelluride; dimethylditellane
• CAS NO: 20334-43-4
• Molecular Formula: C₂H₆Te₂
• Molecular Weight: 285.269
• EINECS: 243-741-7
• Mol File: 20334-43-4.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: dimethyl ditelluride(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl ditelluride(20334-43-4)
• EPA Substance Registry System: dimethyl ditelluride(20334-43-4)

Safety Data

• Hazardous Substances Data: 20334-43-4(Hazardous Substances Data)

Upstream product

• 75-09-2 dichloromethane 
• 474094-06-9 ethyl 2-methyl-2-methyl tellurium propionate 
• 917-54-4 methyllithium 
• 75-34-3 1,1-dichloroethane 
• 74-88-4 methyl iodide 
• 7101-31-7 dimethyl diselenide 
• 14683-12-6 tellurium 
• 107-06-2 1,2-dichloro-ethane 
• 109-70-6 1.3-chlorobromopropane 
• 2229-07-4 methyl radical 
• 105679-05-8 methanetellurinic acid-anhydride 
• 77-78-1 dimethyl sulfate 
• 74-83-9 methyl bromide 

Downstream Products

• 105598-32-1 1,3-bis(methyltelluranyl)propane 
• 114438-52-7 methyl(allyl)telluride 
• 291-25-8 1,3,5-triselenacyclohexane 
• 100207-53-2 bis(methyltellanyl)methane 
• 593-80-6 dimethyltellurium 
• 1025398-97-3 (4S,5R)-5-{[(4,4'-dimethoxytrityl)oxy]methyl}-4,5-dihydrofuran-4-ol 
• 1198293-46-7 2'-deoxy-2'-methyltellanyl-5'-O-(4,4'-dimethoxytrityl)uridine 
• 1198293-47-8 2'-deoxy-2'-methyltellanyl-5'-O-(4,4'-dimethoxytrityl)thymidine 
• 1221001-23-5 1,1-bis(methyltellanyl)ethane 
• 79971-49-6 methyl ethyl ditelluride 
• 120058-46-0 methyl o-(dimethylstibino)phenyl telluride 
• 19859-25-7 1-methyltelluro-2-phenylethyne 
• 74185-36-7 2-((Z)-2-Methyltellanyl-vinyl)-benzoic acid ethyl ester 
• 32294-60-3 diphenyl ditelluride 

Relevant articles and documents

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Synthesis of 1,2-ditellurane

Freshly prepared solutions of disodium ditelluride react with diiodobutane to give small yields of 1,2-ditellurane.In contrast, reactions of α,α-bis(chloromethyl)-o-xylene and phthaloyl chloride give 3,4-benzo-1-telluracyclopentane and tellurophthalic anhydride respectively.

THE PREPARATION OF DI-t-BUTYL DITELLURIDE AND DI-t-BUTYL TELLURIDE AND THE 125Te NMR AND MOESSBAUER SPECTRA OF SOME DIALKYL TELLURIDES AND DITELLURIDES

The synthesis of di-t-butyl ditelluride, t-Bu2Te2, an di-t-butyl telluride, t-Bu2Te, are reported together with that of di-(neo-hexyl) ditelluride.New syntheses of Me2Te2 and i-Pr2Te2 are presented.The high resolution 125Te NMR data and the Moessbauer data for these compounds are discussed.The use of tellurium-proton couplings in high resolution 125Te NMR spectra in assigning the resonances in mixed dialkyl ditellurides is also illustrated.

RADICAL POLYMERIZATION INITIATOR AND METHOD FOR PRODUCING POLYMERS

The present invention involves a radical polymerization initiator comprising an organotellurium compound represented by a formula (1), wherein R1 represents an alkyl group or the like, each of R2 and R3 independently represents a hydrogen atom or the like, and each of R4, R5, and R6 independently represents a hydrogen atom or the like. The present invention provides: a radical polymerization initiator that is useful for producing a polymer that includes a double bond at the molecular terminal; and a method for producing a polymer that utilizes the radical polymerization initiator.