Conditions | Yield |
---|---|
With graphene immobilized iridium complex containing N-heterocyclic carbene ligand functionalized with pyrene at 30℃; for 0.5h; | 97% |
Triethoxysilane
Triethoxyvinylsilane
A
1,2-bis(triethoxysilyl)ethane
B
1,2-bis(triethoxysilyl)ethylene
Conditions | Yield |
---|---|
With ruthenium acetylacetonate for 2h; Heating; | A 90% B 2% |
With tris(triphenylphosphine)ruthenium(II) chloride for 0.5h; Heating; | A 46% B 14% |
Conditions | Yield |
---|---|
With hydrogenchloride at 60 - 120℃; for 3h; Temperature; Inert atmosphere; | 87% |
In dichloromethane at 50℃; for 0.5h; | 86% |
Triethoxysilane
acetylene
A
Triethoxyvinylsilane
B
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With bis(triphenylphosphine)platinum(II) dichloride In benzene at 80℃; for 10h; Product distribution; other hydrosilanes; var. group-VIII metal phosphine complexes as catalysts, var. solvents, var. conc., var. temperatures and times; | A 86% B 3 % Chromat. |
With bis(triphenylphosphine)platinum(II) dichloride In benzene at 80℃; for 10h; | A 86% B 3 % Chromat. |
With dihydrogen hexachloroplatinate In benzene at 40℃; for 1h; | A 36% B 30% |
Conditions | Yield |
---|---|
Platinum catalyst II at 110 - 120℃; for 7h; | 77% |
With dihydrogen hexachloroplatinate In benzene for 24h; | 76% |
dichlorobis(diethyl sulfide)platinum In benzene at 120℃; for 48h; | 58% |
Conditions | Yield |
---|---|
Rh(I)-catalyst In tetrahydrofuran for 1h; Ambient temperature; Yields of byproduct given; | A 50% B n/a |
Rh(I)-catalyst In tetrahydrofuran for 1h; Ambient temperature; Yield given; | A 50% B n/a |
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 50 - 60℃; for 4h; |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
tetraethoxy orthosilicate
C
1,2-bis(triethoxysilyl)ethane
D
1,2-bis(triethoxysilyl)ethylene
E
1,4-bis(triethoxysilyl)butane
F
C16H38O6Si2
Conditions | Yield |
---|---|
With air; triphenylphosphine; bis(acetylacetonate)nickel(II) In hexane for 0.25h; Product distribution; other temp.; other reaction time; | A 10% B 16% C 3% D 31% E 34% F 3% |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
tetraethoxy orthosilicate
C
1,2-bis(triethoxysilyl)ethane
D
1,4-bis(triethoxysilyl)butane
E
C16H38O6Si2
F
(E)-1,2-bis(triethoxysilyl)ethylene
Conditions | Yield |
---|---|
bis(acetylacetonate)nickel(II) for 0.25h; Product distribution; Heating; var. temp., times; | A 11% B 14% C 7% D 21% E 7% F 32% |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
1,2-bis(triethoxysilyl)ethane
C
1,2-bis(triethoxysilyl)ethylene
Conditions | Yield |
---|---|
With bis(acetylacetonate)nickel(II) at 120℃; for 2h; | A n/a B 6% C 10% D 29% |
With bis(acetylacetonate)nickel(II) at 60℃; for 2h; Product distribution; other trialkoxysilanes and vinyltrialkoxysilanes, other transition metal complexes, var. temp. and times; | A n/a B 6% C 13% D 21% |
Conditions | Yield |
---|---|
With di(rhodium)tetracarbonyl dichloride at 45℃; for 2h; | 28% |
In neat (no solvent) HSi(OC2H5)3 and C2H2 on Pt at about 300°C under pressure;; | |
In neat (no solvent) HSi(OC2H5)3 and C2H2 on Pt at about 300°C under pressure;; |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
1,2-bis(triethoxysilyl)ethane
C
1,2-bis(triethoxysilyl)ethylene
D
1,4-bis(triethoxysilyl)butane
E
C16H38O6Si2
Conditions | Yield |
---|---|
With bis(acetylacetonate)nickel(II) at 120℃; for 2h; Product distribution; other trisubstituted silanes and vinyl-trisubstituted silanes, other temp. and time; | A 12 % Chromat. B 11 % Chromat. C 48 % Chromat. D 22 % Chromat. E 2 % Chromat. F 4 % Chromat. |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
1,2-bis(triethoxysilyl)ethane
C
1,2-bis(triethoxysilyl)ethylene
D
1,4-bis(triethoxysilyl)butane
Conditions | Yield |
---|---|
bis(acetylacetonate)nickel(II); triphenylphosphine for 2h; Product distribution; Heating; var. time; Ni(0) and Ni(II) phosphine and non phosphine complexes as catalysts; | A 14 % Chromat. B n/a C 3 % Chromat. D n/a E n/a F 20 % Chromat. |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
1,2-bis(triethoxysilyl)ethane
C
1,4-bis(triethoxysilyl)butane
Conditions | Yield |
---|---|
bis(acetylacetonate)nickel(II); tricyclohexylphosphine at 120℃; for 40h; Further byproducts given; | A 14 % Chromat. B 13 % Chromat. C 20 % Chromat. D 35 % Chromat. |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
1,2-bis(triethoxysilyl)ethane
C
1,4-bis(triethoxysilyl)butane
Conditions | Yield |
---|---|
bis(acetylacetonate)nickel(II) for 2h; Heating; Further byproducts given; | A 15 % Chromat. B 28 % Chromat. C 22 % Chromat. D 20 % Chromat. |
Conditions | Yield |
---|---|
With Pt(PPh3)2(CH=CH2) at 110℃; for 6h; Product distribution; other silane, olefin and platinum complexes; var. temp. and time; |
ethene
Triethoxysilane
A
ethyltriethoxy silane
B
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
at 130℃; |
Triethoxysilane
acetylene
A
Triethoxyvinylsilane
B
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
at 130℃; under 14710.2 Torr; |
Triethoxysilane
Triethoxyvinylsilane
A
ethyltriethoxy silane
B
1,2-bis(triethoxysilyl)ethane
C
1,4-bis(triethoxysilyl)butane
D
(E)-1,2-bis(triethoxysilyl)ethylene
Conditions | Yield |
---|---|
[{Ni(η-CH2=CHSiMe2)2O}2{μ-(η-CH2=CHSiMe2)2O}] at 120℃; for 2h; dehydrogenative coupling; Further byproducts given; |
chloromethyltriethoxysilane
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With aluminium trichloride at 110 - 120℃; for 3h; | 19 % Chromat. |
1,2-bis(trichlorosilyl)ethane
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With ethanol | |
With C2H5OH |
Triethoxysilane
acetylene
A
ethyltriethoxy silane
B
Triethoxyvinylsilane
C
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 5℃; for 6h; | A 7 %Spectr. B 70 %Spectr. C 15 %Spectr. |
Triethoxysilane
acetylene
A
ethyltriethoxy silane
B
Triethoxyvinylsilane
C
1,2-bis(triethoxysilyl)ethane
D
1,2-bis(triethoxysilyl)ethylene
Conditions | Yield |
---|---|
With hexachloroplatinic(IV) acid hydrate at 25℃; for 3h; | A 8 %Spectr. B 49 %Spectr. C 19 %Spectr. D 5 %Spectr. |
ethanol
1,2-bis(trichlorosilyl)ethane
1,2-bis(trichlorosilyl)ethene
Trichloro-silylethene
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
Stage #1: ethanol; 1,2-bis(trichlorosilyl)ethane; 1,2-bis(trichlorosilyl)ethene; trichloroethylsilane; Trichloro-silylethene In toluene at 50 - 60℃; for 1h; Inert atmosphere; Reflux; Stage #2: With hydrogen; palladium 10% on activated carbon In ethanol at 80℃; under 3750.38 Torr; for 4h; |
1,2-bis(triethoxysilyl)ethylene
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With hydrogen; palladium 10% on activated carbon In ethanol under 750.075 Torr; for 1h; |
Conditions | Yield |
---|---|
With di-tert-butyl peroxide at 20℃; for 1h; |
triisopropanolamine
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With potassium hydroxide In toluene at 100℃; under 100 - 760 Torr; for 4h; | 94% |
With potassium hydroxide at 220℃; | 38% |
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With ammonium hydrogen difluoride In water at 20℃; | 81% |
1,2-bis(triethoxysilyl)ethane
1,3,5,7,9,11,14-heptacyclopentyltricyclo[7.3.3.15,11]heptasiloxane-endo-3,7,14-triol
Conditions | Yield |
---|---|
With tetramethyl ammoniumhydroxide In methanol; ethanol at 0 - 5℃; for 24h; Cooling with ice; | 77.5% |
1,2-bis(triethoxysilyl)ethane
allylmagnesium bromide
1,2-bis[ethoxydi(prop-2-enyl)silyl]ethane
Conditions | Yield |
---|---|
In diethyl ether at 0 - 20℃; for 10h; | 75% |
triethanolamine
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With potassium hydroxide at 220℃; | 43% |
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With potassium hydroxide at 220℃; | 36% |
1,2-bis(triethoxysilyl)ethane
triethanolamine
Conditions | Yield |
---|---|
In xylene for 75h; Heating; | 24.3% |
1,2-bis(triethoxysilyl)ethane
methylmagnesium bromide
Si,Si'-diethoxy-Si,Si,Si',Si'-tetramethyl-Si,Si'-ethanediyl-bis-silane
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With hydrogenchloride; water In ethanol for 24h; Yield given; |
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With hydrogenchloride; Brij 76 at 50 - 90℃; for 48h; |
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
With hydrogenchloride; triblock copolymer EO20PO70EO20 at 40 - 100℃; for 144h; | |
With hydrogenchloride; triblock copolymer EO20PO70EO20 at 40 - 100℃; for 168h; |
1,2-bis(triethoxysilyl)ethane
3-(trimethoxysilyl)-1-propanethiol
The 1,2-Bis(triethoxysilyl)ethane, with the CAS registry number 16068-37-4, is also known as [(Triethoxysilyl)ethyl]triethoxysilane. It belongs to the product categories of Industrial/Fine Chemicals; Bridged Monomers Self Assembly & Contact Printing; Silane Coupling Agents/Adhesion Promoters; Tri-Alkoxy & Greater Silanes Organometallic Reagents; Organosilicon; Self-Assembly Materials; Trialkoxysilanes. Its EINECS number is 240-212-2. This chemical's molecular formula is C14H34O6Si2 and molecular weight is 354.59. What's more, its systematic name is 4,4,7,7-Tetraethoxy-3,8-dioxa-4,7-disiladecane. Its classification codes are: (1)TSCA Flag P [A commenced PMN (Premanufacture Notice)substance]; (2)TSCA Flag S [Substance is identified in a proposed or final SNUR (Significant New Use Rule)under TSCA].
Physical properties of 1,2-Bis(triethoxysilyl)ethane are: (1)ACD/LogP: 5.469; (2)# of Rule of 5 Violations: 1; (3)ACD/LogD (pH 5.5): 5.47; (4)ACD/LogD (pH 7.4): 5.47; (5)ACD/BCF (pH 5.5): 8441.22; (6)ACD/BCF (pH 7.4): 8441.22; (7)ACD/KOC (pH 5.5): 22496.29; (8)ACD/KOC (pH 7.4): 22496.29; (9)#H bond acceptors: 6; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 15; (12)Polar Surface Area: 55.38 Å2; (13)Index of Refraction: 1.427; (14)Molar Refractivity: 94.815 cm3; (15)Molar Volume: 369.278 cm3; (16)Polarizability: 37.587×10-24cm3; (17)Surface Tension: 24.97 dyne/cm; (18)Density: 0.96 g/cm3; (19)Flash Point: 125.35 °C; (20)Enthalpy of Vaporization: 53.4 kJ/mol; (21)Boiling Point: 314.956 °C at 760 mmHg; (22)Vapour Pressure: 0.001 mmHg at 25°C.
When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. When using it, you need wear suitable protective clothing. In case of fire and/or explosion, you should not breathe fumes.
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