4551-16-0

Basic information

• Product Name: (BIS(TRIMETHYLSILYL))TELLURIDE
• Synonyms: Bis(trimethylsilyl)tellurium;Disilatellurane,hexamethyl-;Disiltellurane,hexamethyl-;hexamethyl-disilatellane;Silane,tellurobis[trimethyl-;(BIS(TRIMETHYLSILYL))TELLURIDE;(BIS(TRIMETHYLSILYL))TELLURIDE 98%;Bis(trimethylsilyl)telluride,98%
• CAS NO: 4551-16-0
• Molecular Formula: C₆H₁₈Si₂Te
• Molecular Weight: 273.98
• Mol File: 4551-16-0.mol
• Article Data: 13

Chemical Properties

• Melting Point: 13.5 °C
• Boiling Point: 74 °C (11 mmHg)
• Appearance: /liquid
• Density: 0.97
• CAS DataBase Reference: (BIS(TRIMETHYLSILYL))TELLURIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (BIS(TRIMETHYLSILYL))TELLURIDE(4551-16-0)
• EPA Substance Registry System: (BIS(TRIMETHYLSILYL))TELLURIDE(4551-16-0)

Safety Data

• Safety Statements: 24/25
• TSCA: No
• Hazardous Substances Data: 4551-16-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H18Si2Te/c1-7(2,3)9-8(4,5)6/h1-6H3

Upstream product

• 75-77-4 chloro-trimethyl-silane 
• 42491-33-8 tert-butylbis(trimethylsilyl)phosphine 
• 17154-34-6 (trimethylsilyl)diphenylphosphine 
• 12034-41-2 disodium telluride 
• 151519-47-0 gold(I) tris(trimethylsilyl)silane telluride 
• 42491-34-9 di-tert-butyl(trimethylsilyl)phosphane 
• 100-58-3 phenylmagnesium bromide 
• 109-99-9 tetrahydrofuran 

Downstream Products

• 14683-12-6 tellurium 
• 935681-87-1 (diphenyl(ethyl)phosphine)3Cu(trimethylsilyltellurolato) 
• 935681-86-0 (diethyl(phenyl)phosphine)3Cu(trimethylsilyltellurolato) 
• 754982-34-8 [Au₄(TeGaCl₃)2((CH₂)6(P(C₆H₅)2)2)2] 

Relevant articles and documents

A N-Heterocyclic Carbene-Stabilized Coinage Metal-Chalcogenide Framework with Tunable Optical Properties

A new class of coinage-metal chalcogenide compounds [Au4M4(μ3-E)4(IPr)4] (M = Ag, Au; E = S, Se, Te) has been synthesized from the combination of N-heterocyclic carbene-ligated gold(I) trimethylsilylc

Synthesis and Thorough Investigation of Discrete Organotin Telluride Clusters

Systematic experimental and theoretical investigations of reactions of R1SnCl3 (R1=CMe2CH2C(Me)O) with (Me3Si)2Te allowed for the stepwise formation and single-crystalline isolation of the first tin sesquitelluride clusters with functional organic ligands. Subsequent derivatization of the latter took place under reorganization of the inorganic core, affording clusters with complex hybrid architectures.

Bis(oligosilanyl)chalcogenides [Me3Si)xMe3-xSi]2E, alkalimetal oligosilanylchalcogenolates (Me3Si)xMe3-xSi-EMI and oligosilanylchalcogenols (Me3Si)xMe3-xSi-EH (E = S, Se, Te) syntheses and NMR study

Bis(oligosilanyl)chalcogenides [(Me3Si)x Me3-x Si]2E, alkalimetal oligosilanylchalcogenolates (Me3Si)x Me3-x Si-EMI and oligosilanylchalcogenols (Me3Si)x Me3-x Si-EH (x=1-3; E=S, Se, Te) were synthesized and characterized by 1H-, 13C-, 29Si-, 77Se- and 125Te-NMR spectroscopy. Trends of NMR parameters (chemical shifts, coupling constants) are discussed.