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Merck

205338

Sigma-Aldrich

Tellurium tetrachloride

99%

Synonim(y):

Tellurium chloride, Tellurium(IV) chloride, Tetrachlorotellurium

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About This Item

Wzór liniowy:
TeCl4
Numer CAS:
Masa cząsteczkowa:
269.41
Numer WE:
Numer MDL:
Kod UNSPSC:
12352302
Identyfikator substancji w PubChem:
NACRES:
NA.23

Próba

99%

Postać

powder, crystals or chunks

tw

380 °C (lit.)

mp

224 °C (lit.)

gęstość

3.26 g/mL at 25 °C (lit.)

ciąg SMILES

Cl[Te](Cl)(Cl)Cl

InChI

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

Klucz InChI

SWLJJEFSPJCUBD-UHFFFAOYSA-N

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Opis ogólny

Atomic number of base material: 52 Tellurium

Zastosowanie

  • 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).
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Piktogramy

Corrosion

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

Skin Corr. 1B

Kod klasy składowania

8A - Combustible corrosive hazardous materials

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

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


Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Klienci oglądali również te produkty

Slide 1 of 2

1 of 2

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
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
P Mareeswari et al.
Enzyme and microbial technology, 95, 225-229 (2016-11-22)
We report an efficient method to biosynthesize biocompatible cadmium telluride and cadmium sulphide quantum dots from the fungus Rhizopus stolonifer. The suspension of the quantum dots exhibited purple and greenish-blue luminescence respectively upon UV light illumination. Photoluminescence spectroscopy, X-ray diffraction
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
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.

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