Conditions | Yield |
---|---|
With potassium hydroxide; tellurium; hydrazine hydrate at 60 - 70℃; | 93% |
Conditions | Yield |
---|---|
With lithium telluride In tetrahydrofuran | 85% |
With sodium hydroxide; tellurium; hydrazine hydrate In N,N-dimethyl-formamide at 60℃; for 0.5h; | 68% |
With tellurium; cetyltrimethylammonim bromide; N,N'-bis[3-(triethylsilyl)propyl]thiocarbamide S,S-dioxide In tetrahydrofuran; sodium hydroxide for 1h; Heating; |
diethyl telluride
Conditions | Yield |
---|---|
With tellurium; naphthalene; sodium In tetrahydrofuran at 0℃; for 0.5h; | 85% |
ethyl bromide
acetylene
A
diethyl telluride
B
divinyltellane
C
vinyl ethyl telluride
Conditions | Yield |
---|---|
With potassium hydroxide; tellurium; tin(ll) chloride In water at 105 - 115℃; under 6080 - 11400 Torr; for 5h; | A 6% B 55% C 69% |
With potassium hydroxide; tellurium; tin(ll) chloride In water at 105 - 115℃; under 11400 Torr; for 5h; | A 6% B 55% C 69% |
With potassium hydroxide; tellurium; tin(ll) chloride; acetylene In water at 105 - 115℃; under 6080 - 11400 Torr; for 5h; | A 10% B 26% C 35% |
Conditions | Yield |
---|---|
With tellurium; hydrazine hydrate; potassium hydroxide at 30 - 35℃; for 9h; | A 8% B 64% |
ammonium O,O-diethyldithiophosphate
triethyltelluronium iodide
A
Et3TeAg4I5
B
diethyl telluride
C
O,O,S-triethyl phosphorodithioate
Conditions | Yield |
---|---|
In water The silver salt of O,O-diethyl dithiophosphate was prepared from equimolar aq. solns. of AgNO3 and NH4(1+){S2P(OEt)2}(1-) and reacted in situ with an aq. soln. of Et3TeI. The react. mixt. was wartmed up to 70°C for ca. 3 h.; React. mixt. cooled to room temp., Et3TeAg4I5 extd. with CH2Cl2 and pptd. with CHCl3; elem.anal.; Et2Te and EtSP(S)(OEt)2 detected in the extn. residue by MS.; | A 50% B n/a C n/a |
Conditions | Yield |
---|---|
at 100 - 110℃; |
Conditions | Yield |
---|---|
at 100 - 110℃; |
ethyl bromide
A
Diethyl disulfide
B
diethyl telluride
C
diethyl ditelluride
Conditions | Yield |
---|---|
With sodium hydroxide; tellurium; sulfur; hydrazine hydrate In water at 35℃; Further byproducts given; | A 21.3 % Chromat. B 4.7 % Chromat. C 37.2 % Chromat. D 5.0 % Chromat. |
ethyl bromide
A
diethyl diselenide
B
diethyl telluride
C
diethyl ditelluride
Conditions | Yield |
---|---|
With sodium hydroxide; tellurium; sulfur; hydrazine hydrate In water at 35℃; Further byproducts given; | A 43.7 % Chromat. B 3.5 % Chromat. C 30.3 % Chromat. D 1.03 % Chromat. |
tellurium tetrachloride
C
diethyl telluride
Conditions | Yield |
---|---|
at 40℃; for 3h; |
ethyl bromide
dichloromethane
A
diethyl telluride
B
diethyl ditelluride
C
2,4-ditellurahexane
Conditions | Yield |
---|---|
Stage #1: dichloromethane With dipotassium telluride; hydrazine hydrate; potassium hydroxide at 20 - 42℃; Stage #2: ethyl bromide at 20 - 38℃; | A 20 %Chromat. B 8 %Chromat. C 8 %Chromat. D 39 %Chromat. |
Conditions | Yield |
---|---|
In benzene-d6 for 72h; |
diethyl telluride
[(η(5)-C5H5)2Rh2(CO)(μ-η(1):η(1)-CF3C2CF3)(TeEt2)]
Conditions | Yield |
---|---|
In dichloromethane stirring (30 min); evapn., chromy. (CH2Cl2 / hexane = 1 : 1), extg. (CH2Cl2), evapn.; elem.anal.; | 100% |
diethyl telluride
Conditions | Yield |
---|---|
In acetonitrile slow addn. of soln. of Ni(SO3Cl)2 in CH3CN to soln. of diethyl telluride in CH3CN under dry N2; stirring magnetically in closed vessel for about 10 h; pptn.;; filtration; washing several times with CH3CN followed by dry Et2O; drying in vac.; elem. anal.;; | 87% |
Conditions | Yield |
---|---|
In pentane refluxed under Ar for 1 wk; filtered, removal of solvent in vac., chromy. on alumina (pentane), removal of solvent; elem. anal.; | 87% |
Conditions | Yield |
---|---|
With HCl In hydrogenchloride; ethanol a soln. of CuCl in dil. HCl was mixed with a soln. of Et2Te in 95% EtOH; ppt. was filtered, washed with EtOH, dried in vacuo, addnl. amts. of the compound sepd. from the filtrate on keeping it overnight; elem. anal.; | 75% |
diethyl telluride
Conditions | Yield |
---|---|
In acetonitrile slow addn. of soln. of Cu(SO3Cl)2 in CH3CN to soln. of diethyl telluride in CH3CN under dry N2; stirring magnetically in closed vessel for about 10 h; pptn.;; filtration; washing several times with CH3CN followed by dry Et2O; drying in vac.; elem. anal.;; | 72% |
dicobalt octacarbonyl
triiron dodecarbonyl
diethyl telluride
Conditions | Yield |
---|---|
High Pressure; high CO pressure; | 30% |
diethyl telluride
diethyl-tellurium oxide
Conditions | Yield |
---|---|
With nitric acid das salpetersaure Salz entsteht; |
o-tetrachloroquinone
diethyl telluride
4,5,6,7-Tetrachloro-2,2-diethyl-2λ4-benzo[1,3,2]dioxatellurole
Conditions | Yield |
---|---|
In toluene at -78℃; for 2h; Yield given; |
diethyl telluride
3,5-di-tert-butyl-o-benzoquinone
4,6-Di-tert-butyl-2,2-diethyl-2λ4-benzo[1,3,2]dioxatellurole
Conditions | Yield |
---|---|
In toluene at -78℃; for 2h; Mechanism; one-electron transfer reaction; also with elemental tellurium and other orthobenzoquinones, other teperatures; | |
In toluene at -78℃; for 2h; Yield given; |
The Diethyl telluride, also known as Ethyl telluride, is an organic compound with the formula C4H10Te. Its EINECS registry number is 211-002-8. With the CAS registry number 627-54-3, its IUPAC name is ethyltellanylethane.
Physical properties of Diethyl telluride: (1)H-Bond Donor: 0; (2)H-Bond Acceptor: 0; (3)Rotatable Bond Count: 2; (4)Exact Mass: 187.984473; (5)MonoIsotopic Mass: 187.984473; (6)Topological Polar Surface Area: 0; (7)Heavy Atom Count: 5; (8)Formal Charge: 0; (9)Complexity: 11.1; (10)Isotope Atom Count: 0; (11)Defined Atom StereoCenter Count: 0; (12)Undefined Atom StereoCenter Count: 0; (13)Defined Bond StereoCenter Count: 0; (14)Undefined Bond StereoCenter Count: 0; (15)Covalently-Bonded Unit Count: 1.
Preparation: this chemical can be prepared by bromoethane. This reaction will need reagents tellurium, sodium hydroxide (powd.), 80percent hydrazine hydrate and solvent dimethylformamide. The reaction time is 30 min with reaction temperature of 60 °C. The yield is about 68%.
Uses of Diethyl telluride: it can be used to produce 1-ethyltellanylmethyl-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol by heating. This reaction will need reagent NaBH4 and solvent ethanol. The yield is about 80%.
When you are using this chemical, please be cautious about it as the following:
This chemical that at low levels can cause damage to health. It is toxic by inhalation, in contact with skin and if swallowed. Whenever you will use it, please wear suitable protective clothing and gloves. In case of accident or if you feel unwell seek medical advice immediately (show the label where possible).
You can still convert the following datas into molecular structure:
(1)Canonical SMILES: CC[Te]CC
(2)InChI: InChI=1S/C4H10Te/c1-3-5-4-2/h3-4H2,1-2H3
(3)InChIKey: ILXWFJOFKUNZJA-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LC50 | inhalation | 117mg/m3 (117mg/m3) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 25(10), Pg. 51, 1981. | |
mouse | LD50 | oral | 154mg/kg (154mg/kg) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 25(10), Pg. 51, 1981. | |
rat | LC50 | inhalation | 24mg/m3 (24mg/m3) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 25(10), Pg. 51, 1981. | |
rat | LD50 | oral | 54100ug/kg (54.1mg/kg) | Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 25(10), Pg. 51, 1981. |
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