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Key Documents

205338

Sigma-Aldrich

Tellurium tetrachloride

99%

Synonyme(s) :

Tellurium chloride, Tellurium(IV) chloride, Tetrachlorotellurium

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About This Item

Formule linéaire :
TeCl4
Numéro CAS:
Poids moléculaire :
269.41
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352302
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Niveau de qualité

Pureté

99%

Forme

powder, crystals or chunks

Point d'ébullition

380 °C (lit.)

Pf

224 °C (lit.)

Densité

3.26 g/mL at 25 °C (lit.)

Chaîne SMILES 

Cl[Te](Cl)(Cl)Cl

InChI

1S/Cl4Te/c1-5(2,3)4

Clé InChI

SWLJJEFSPJCUBD-UHFFFAOYSA-N

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Description générale

Atomic number of base material: 52 Tellurium

Application

  • Highly efficient regioselective synthesis of organotellurium compounds: Explores the reactions of Tellurium Tetrachloride with 1-alkenes, highlighting its utility in organic synthesis (VA Potapov et al., 2017).
  • Cyclization Reactions: TeCl4 acts as a bis-electrophile in double-electrophilic cyclization reactions, demonstrating its versatility in organic transformations (N Korol, M Slivka, 2018).
  • Regio-and stereoselective addition of tellurium tetrachloride: Investigates the addition of TeCl4 to methyl propargyl ether, emphasizing the stereochemistry of the addition process (MV Musalova et al., 2017).

Pictogrammes

Corrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Skin Corr. 1B

Code de la classe de stockage

8A - Combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Certificats d'analyse (COA)

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Les clients ont également consulté

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Shalini Roy et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 49(10), 2564-2574 (2011-07-12)
Tellurium tetrachloride (TeCl(4)) and diphenyl ditelluride (DPDT) cytotoxicity, was investigated in rat astrocytes. Concentrations of 0.24-250μM (24h) were tested for viability using MTT(3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide) and trypan blue exclusion. MTT showed significant decreases at all concentrations tested for both compounds.
Maria V Musalova et al.
Molecules (Basel, Switzerland), 17(5), 5770-5779 (2012-05-17)
The reaction of tellurium tetrachloride with acetylene proceeds in a stereospecific anti-addition manner to afford the novel products E-2-chlorovinyltellurium trichloride and E,E-bis(2-chlorovinyl)tellurium dichloride. Reaction conditions for the selective preparation of each of these products were found. The latter was obtained
Kyoko Iwase et al.
Environmental toxicology, 19(6), 614-619 (2004-11-05)
Despite the growing use of organotellurium compounds in the chemical and biomedical fields, there has been no great concern about their toxicity until now. To test the possibility that diphenyl ditelluride (DPDT) and tellurium chloride (TeCl2), organic and inorganic tellurium
J F Van Vleet et al.
American journal of veterinary research, 43(11), 2000-2009 (1982-11-01)
Seventy newly hatched ducklings were fed a commercial ration with 500 mg of added Te (as tetrachloride)/kg of feed for up to 28 days. Ducklings were euthanatized at day 14, 21, and 28, the hearts were studied by gross, microscopic
Puneet Vij et al.
Environmental toxicology and pharmacology, 34(3), 768-782 (2012-10-17)
Diphenyl ditelluride (DPDT) and tellurium tetrachloride (TeCl(4)) were evaluated for toxicity in transformed (HT-29, Caco-2) and non-transformed colon cells (CCD-18Co). Significant decreases in viability were observed with DPDT exposure in HT-29 (62.5-1000 μM), Caco-2 (31.25-1000 μM) and CCD-18Co cells (500-1000

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