Conditions | Yield |
---|---|
In dichloromethane at 50 - 80℃; for 3h; | 99% |
In dichloromethane at 50℃; | 78% |
With tin(IV) chloride; cyclohexene for 1h; Ambient temperature; | 73.4% |
Conditions | Yield |
---|---|
at 90℃; under 225.023 - 375.038 Torr; Temperature; | 96.7% |
With acetylacetonatodicarbonylrhodium(l) for 2h; the temperature did not rise above 45 deg C; | 70% |
With cyclopentadienylruthenium(II) trisacetonitrile hexafluorophosphate at 25℃; for 2h; | 95 %Spectr. |
With platinum on activated charcoal at 130℃; under 14710.2 Torr; |
tetraethoxy orthosilicate
trichlorovinylsilane
A
Triethoxyvinylsilane
B
vinyldi(ethoxy)chlorosilane
C
vinyl(ethoxy)dichlorosilane
Conditions | Yield |
---|---|
at 20 - 22℃; for 150h; | A 2% B 95% C 1% |
ethanol
trichlorovinylsilane
A
Triethoxyvinylsilane
B
1,3-diivinyl-1,1,3,3-tetraethoxydisiloxane
Conditions | Yield |
---|---|
In diethyl ether at 45 - 80℃; for 3h; Product distribution; different chlorosilanes, alcohols, solvents and reaction temperatures; | A 92.9% B 5.5% |
ethene
Triethoxysilane
A
ethyltriethoxy silane
B
Triethoxyvinylsilane
Conditions | Yield |
---|---|
With FeBr2(iPrPQpy); lithium triethylborohydride In toluene at 70℃; under 1520.1 Torr; for 2h; Inert atmosphere; Glovebox; Schlenk technique; | A 10% B 90% |
With lithium triethylborohydride In toluene at 70℃; under 1520.1 Torr; for 2h; Inert atmosphere; Glovebox; Schlenk technique; | A 60% B 40% |
With FeBr2(iPrPQpy); sodium triethylborohydride In toluene at 70℃; under 1520.1 Torr; for 2h; Catalytic behavior; Reagent/catalyst; Cooling; |
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% |
ethene
1,1,1,3,5,5,5-heptamethyltrisiloxan
A
ethyltriethoxy silane
B
Triethoxyvinylsilane
Conditions | Yield |
---|---|
With CoCl2(iPrPQpy); lithium triethylborohydride In toluene at 70℃; under 1520.1 Torr; for 2h; Inert atmosphere; Glovebox; Schlenk technique; | A 86% B 14% |
Conditions | Yield |
---|---|
With C2H5OH; pyridine | 60.1% |
With C2H5OH | 50.4% |
Triethoxysilane
acetylene
A
Triethoxyvinylsilane
B
(E)-1,2-bis(triethoxysilyl)ethylene
Conditions | Yield |
---|---|
With {palladium-dichloro-(P(C3H7)3)2} In xylene at 80℃; for 3h; | A 54% B 9% |
tetraethoxy orthosilicate
trichlorovinylsilane
A
trichloroethoxysilane
B
dichlorodiethoxysilane
C
chlorotriethoxysilane
D
Triethoxyvinylsilane
E
vinyldi(ethoxy)chlorosilane
F
vinyl(ethoxy)dichlorosilane
Conditions | Yield |
---|---|
N,N-dimethyl-formamide at 90℃; for 5.5h; Product distribution; Thermodynamic data; Equilibrium constant; ΔG0, ΔH0; |
ethanol
trichlorovinylsilane
A
ethyl trimethylsilyl ether
B
Triethoxyvinylsilane
C
vinyldi(ethoxy)chlorosilane
D
vinyl(ethoxy)dichlorosilane
Conditions | Yield |
---|---|
With chloro-trimethyl-silane for 1h; Ambient temperature; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts; |
ethanol
trichlorovinylsilane
A
Triethoxyvinylsilane
B
vinyldi(ethoxy)chlorosilane
C
vinyl(ethoxy)dichlorosilane
Conditions | Yield |
---|---|
With chloro-trimethyl-silane for 1h; Product distribution; Ambient temperature; various educt ratios; |
Triethoxysilane
acetylene
A
Triethoxyvinylsilane
B
1,2-bis(triethoxysilyl)ethane
Conditions | Yield |
---|---|
at 130℃; under 14710.2 Torr; |
Conditions | Yield |
---|---|
at 20℃; Kinetics; Equilibrium constant; |
A
Triethoxyvinylsilane
B
tris(2-aminoethoxy)(vinyl)silane
Conditions | Yield |
---|---|
at 60℃; Equilibrium constant; |
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. |
Triethoxysilane
acetylene
A
Triethoxyvinylsilane
B
1,2-bis(triethoxysilyl)ethylene
Conditions | Yield |
---|---|
With chloro(1,5-cyclooctadiene)rhodium(I) dimer at 25℃; for 18h; | A 74 %Spectr. B 7 %Spectr. |
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 17h; Inert atmosphere; Schlenk technique; | A n/a B 88 %Chromat. |
(E)-1,2-bis(triethoxysilyl)ethylene
diethylamine
A
Triethoxyvinylsilane
B
N-(triethoxysilyl)diethylamine
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 24h; Inert atmosphere; Schlenk technique; | A n/a B 86 %Chromat. |
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 24h; Inert atmosphere; Schlenk technique; | A n/a B 88 %Chromat. |
(E)-1,2-bis(triethoxysilyl)ethylene
N-ethyl-N-phenylamine
A
Triethoxyvinylsilane
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 48h; Inert atmosphere; Schlenk technique; | A n/a B 90 %Chromat. |
(E)-1,2-bis(triethoxysilyl)ethylene
aniline
A
Triethoxyvinylsilane
B
N-phenyl-1,1,1-triethoxysilanamine
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 48h; Inert atmosphere; Schlenk technique; | A n/a B 95 %Chromat. |
(E)-1,2-bis(triethoxysilyl)ethylene
isopropylamine
A
Triethoxyvinylsilane
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 17h; Inert atmosphere; Schlenk technique; | A n/a B 94 %Chromat. |
2,2-dimethylpropylamine
(E)-1,2-bis(triethoxysilyl)ethylene
A
Triethoxyvinylsilane
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In toluene at 120℃; for 24h; Inert atmosphere; Schlenk technique; | A n/a B 92 %Chromat. |
N-deuterio-diethylamine
(E)-1,2-bis(triethoxysilyl)ethylene
A
ethene
B
Triethoxyvinylsilane
Conditions | Yield |
---|---|
With carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In (2)H8-toluene; toluene |
Conditions | Yield |
---|---|
With potassium hydroxide at 240℃; for 3h; Autoclave; Molecular sieve; |
2-Acetylthiophene
Triethoxyvinylsilane
2-acetyl-3-<2-(triethoxysilyl)ethyl>thiophene
Conditions | Yield |
---|---|
With sodium formate; triphenylphosphine; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In toluene at 140℃; for 2h; Murai reaction; | 100% |
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium formate; triphenylphosphine In toluene at 140℃; for 2h; | 100% |
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene for 1h; Heating; | 93% |
With rhodium(III) chloride hydrate; sodium formate; tris(para-trifluoromethyl)phenyl phosphine In 1,4-dioxane at 80℃; for 20h; Inert atmosphere; | 90% |
With [RhCl2(p-cymene)]2; sodium formate; triphenylphosphine In isopropyl alcohol; acetone at 80℃; Inert atmosphere; | 70% |
1'-naphthacetophenone
Triethoxyvinylsilane
2'-<2-(triethoxysilyl)ethyl>-1'-acetonaphthone
Conditions | Yield |
---|---|
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium formate; triphenylphosphine In toluene at 140℃; for 0.3h; | 100% |
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene for 6h; Heating; | 67% |
With bis(1,5-cyclooctadiene)iridium(I) tetrakis[3,5-bis(trifluoromethyl)phenyl]borate; C38H28P2 In 1,3-dioxane at 130℃; for 24h; Reagent/catalyst; regioselective reaction; | 45% |
Triethoxyvinylsilane
3,4-dihydronaphthalene-1(2H)-one
8-(2-triethoxysilyl-ethyl)-3,4-dihydro-2H-naphthalen-1-one
Conditions | Yield |
---|---|
With sodium formate; triphenylphosphine; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In toluene at 140℃; Murai reaction; | 100% |
With (HCHO+4PPh3)-Ru(II) supported on CeO2 In toluene at 140℃; for 0.5h; Inert atmosphere; Schlenk technique; | 99% |
With carbonyldihydridotris(triphenylphosphine)ruthenium(II) In toluene at 125℃; for 0.5h; Inert atmosphere; | 96% |
Triethoxyvinylsilane
2-Methylacetophenone
1-[6-methyl-2-(2-(triethoxysilyl)ethyl)phenyl]-ethanone
Conditions | Yield |
---|---|
[Ru(H2)(CO)(PPh3)3] In toluene at 135℃; for 2h; Addition; | 100% |
carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene for 2h; Heating; other catalysts: Ru(CO)2(PPh3)3, RuH2(PPh3)4, Ru(CO)3(PPh3)2; | 93% |
With rhodium(III) chloride hydrate; sodium formate; tris(para-trifluoromethyl)phenyl phosphine In 1,4-dioxane at 80℃; for 20h; Inert atmosphere; | 67% |
Triethoxyvinylsilane
1-(2-(((1,1-dimethylethyl)dimethylsilyl)oxy)phenyl)ethanone
Conditions | Yield |
---|---|
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) for 12h; | 100% |
carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene for 12h; Heating; | 100% |
Conditions | Yield |
---|---|
carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene at 135℃; for 24h; Addition; | 100% |
Conditions | Yield |
---|---|
carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene at 135℃; for 24h; Addition; | 100% |
Conditions | Yield |
---|---|
carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene at 135℃; for 16h; Addition; | 100% |
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) | 100% |
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene at 135℃; for 24h; regioselective reaction; | 100% |
Triethoxyvinylsilane
Cyclohexyl phenyl ketone
cyclohexyl-{2-[(2-triethoxysilyl)-ethyl]phenyl}methanone
Conditions | Yield |
---|---|
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium formate; triphenylphosphine In toluene at 140℃; for 1h; | 100% |
Triethoxyvinylsilane
acetophenone
1-[2-[2-(triethoxysilyl)ethyl]phenyl]ethanone
Conditions | Yield |
---|---|
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium formate; triphenylphosphine In toluene at 140℃; for 1h; | 100% |
With [Ru(OCOH)2PPh3(p-cym)]; triphenylphosphine In isopropyl alcohol at 80℃; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
With palladium diacetate; sodium hydroxide In water at 140℃; for 3h; Reagent/catalyst; Temperature; Concentration; Hiyama Coupling; | 100% |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) at 80℃; for 4h; Inert atmosphere; Reflux; | 99.5% |
Conditions | Yield |
---|---|
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene for 4h; Heating; | 99% |
methyl cyclohex-1-ene-1-carboxylate
Triethoxyvinylsilane
methyl 2-(2-(triethoxysilyl)ethyl)cyclohex-1-enecarboxylate
Conditions | Yield |
---|---|
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium formate; tris(para-trifluoromethyl)phenyl phosphine In 1,4-dioxane at 20 - 100℃; Inert atmosphere; | 99% |
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene for 18h; | 97% |
Conditions | Yield |
---|---|
[1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(O-isopropoxyphenylmethylene)ruthenium In dichloromethane at 40℃; for 1h; | 99% |
Conditions | Yield |
---|---|
[1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(O-isopropoxyphenylmethylene)ruthenium In dichloromethane at 40℃; for 1h; | 99% |
1,4-benzodioxan-6-yl methyl ketone
Triethoxyvinylsilane
1-[5-(2-triethoxysilyl-ethyl)-2,3-dihydro-benzo[1,4]dioxin-6-yl]ethanone
Conditions | Yield |
---|---|
With sodium formate; triphenylphosphine; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In toluene at 140℃; for 1.5h; Murai reaction; | 99% |
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium formate; triphenylphosphine In toluene at 140℃; for 1.5h; | 99% |
Triethoxyvinylsilane
2-(2-triethoxysilyl-ethyl)naphthalene-1-carbaldehyde
Conditions | Yield |
---|---|
With sodium formate; triphenylphosphine; [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 In toluene at 140℃; | 99% |
Triethoxyvinylsilane
(E)-N-tert-butyl-2-methyl-2-butenamide
(Z)-N-tert-butyl-2,3-dimethyl-5-(triethoxysilyl)pent-2-enamide
Conditions | Yield |
---|---|
With [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2; sodium formate; tris(para-trifluoromethyl)phenyl phosphine In 1,4-dioxane at 20 - 100℃; Inert atmosphere; | 99% |
styrene
Triethoxyvinylsilane
1-styryltriethoxysilane
Conditions | Yield |
---|---|
With [(H2IMes)(OSiMe3)2Ru(=CHC6H4(O-i-Pr)-2)] In dichloromethane for 24h; Reflux; Inert atmosphere; | 99% |
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In toluene at 25℃; for 2h; |
Conditions | Yield |
---|---|
With dihydridotetrakis(triphenylphosphine)ruthenium In toluene at 140℃; for 24h; Inert atmosphere; Schlenk technique; | 99% |
Conditions | Yield |
---|---|
With dihydridotetrakis(triphenylphosphine)ruthenium In toluene at 140℃; for 24h; Inert atmosphere; Schlenk technique; | 99% |
Triethoxyvinylsilane
phenyl-N-(1-naphthylethylidene)methanamine
Conditions | Yield |
---|---|
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene at 140℃; for 72h; Reagent/catalyst; Inert atmosphere; Schlenk technique; | 99% |
Triethoxyvinylsilane
Conditions | Yield |
---|---|
With carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) for 36h; | 98% |
Triethoxyvinylsilane
methyl 13-acetyl-12-(((1,1-dimethylethyl)dimethylsilyl)oxy)podocarpa-8,11,13-trien-19-oate
Conditions | Yield |
---|---|
carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II) In toluene for 36h; Heating; | 98% |
Conditions | Yield |
---|---|
Grubbs catalyst first generation at 60℃; for 24h; cross-metathesis; Title compound not separated from byproducts; | A n/a B 98% |
Triethoxyvinylsilane
ethyl 5-hydroxy-3-keto-hept-6-enoate
ethyl (6E)-8,8,8-triethoxy-5-hydroxy-3-oxo-8-silaoct-6-enoate
Conditions | Yield |
---|---|
With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride In dichloromethane at 45℃; for 1h; | 98% |
3-bromoquinoline
Triethoxyvinylsilane
(E)-1,2-di(quinoline-3-yl)ethene
Conditions | Yield |
---|---|
With sodium hydroxide; palladium diacetate In water at 140℃; for 3h; | 98% |
Stage #1: Triethoxyvinylsilane With sodium hydroxide In water at 20℃; for 0.0833333h; Sealed tube; Stage #2: 3-bromoquinoline With palladium diacetate In water at 120 - 140℃; Sealed tube; | 98% |
With palladium diacetate; sodium hydroxide In water at 140℃; for 4h; Sealed tube; | 91% |
With palladium diacetate; sodium hydroxide In water at 140℃; Hiyama Coupling; Sealed tube; | 91% |
With palladium diacetate; sodium hydroxide In neat (no solvent) at 140℃; for 6h; Hiyama Coupling; Sealed tube; | 91% |
Triethoxyvinylsilane
para-bromoacetophenone
(E)-1,1'-(ethene-1,2-diylbis(4,1-phenylene))diethanone
Conditions | Yield |
---|---|
With sodium hydroxide; palladium diacetate In water at 140℃; for 3h; | 98% |
Stage #1: Triethoxyvinylsilane With sodium hydroxide In water at 20℃; for 0.0833333h; Sealed tube; Stage #2: para-bromoacetophenone With palladium diacetate In water at 120 - 140℃; Sealed tube; | 98% |
Molecule structure of Triethoxyvinylsilane (CAS NO.78-08-0):
IUPAC Name: Ethenyl(triethoxy)silane
Molecular Weight: 190.31222 g/mol
Molecular Formula: C8H18O3Si
Density: 0.904 g/cm3
Melting Point: <0 °C
Boiling Point: 160.5 °C at 760 mmHg
Flash Point: 34.4 °C
Index of Refraction: 1.415
Molar Refractivity: 52.78 cm3
Molar Volume: 210.5 cm3
Surface Tension: 22.3 dyne/cm
Enthalpy of Vaporization: 38.08 kJ/mol
Vapour Pressure: 3.09 mmHg at 25 °C
Storage Temp.: flammables area
Water Solubility: decomposes
Sensitive Moisture: sensitive
H-Bond Acceptor: 3
Rotatable Bond Count: 7
Exact Mass: 190.102521
MonoIsotopic Mass: 190.102521
Topological Polar Surface Area: 27.7
Heavy Atom Count: 12
Canonical SMILES: CCO[Si](C=C)(OCC)OCC
InChI: InChI=1S/C8H18O3Si/c1-5-9-12(8-4,10-6-2)11-7-3/h8H,4-7H2,1-3H3
InChIKey: FWDBOZPQNFPOLF-UHFFFAOYSA-N
EINECS: 201-081-7
Product Categories: Vinyl;Silicone series;Functional Materials;Si (Classes of Silicon Compounds);Silane Coupling Agents;Si-O Compounds;Trialkoxysilanes;Vinyl Silanes (Silane Coupling Agents);Vinylsilanes, Allylsilanes;Adhesion Promoters;Coupling Agents;Surface Modifiers;Silane series
Triethoxyvinylsilane (CAS NO.78-08-0) is used in silane cross-linked polyethylene cables and pipes. It is also used as hydrophobic agent and the glass fiber surface treatment agent.
1. | skn-rbt 500 mg open MLD | UCDS** Union Carbide Data Sheet. (Industrial Medicine and Toxicology Dept., Union Carbide Corp., 270 Park Ave., New York, NY 10017) 7/10 ,1967. | ||
2. | eye-rbt 500 mg | AMIHBC AMA Archives of Industrial Hygiene and Occupational Medicine. 10 (1954),61. | ||
3. | orl-rat LD50:22,500 mg/kg | AMIHBC AMA Archives of Industrial Hygiene and Occupational Medicine. 10 (1954),61. | ||
4. | ihl-rat LCLo:4000 ppm/4H | AMIHBC AMA Archives of Industrial Hygiene and Occupational Medicine. 10 (1954),61. |
Reported in EPA TSCA Inventory.
Hazard Codes: Xi
Risk Statements: 10-36/37
R10:Flammable.
R36/37:Irritating to eyes and respiratory system.
Safety Statements: 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
RIDADR: UN 1993 3/PG 3
WGK Germany: 2
RTECS: VV6700000
F: 21
TSCA: Yes
HazardClass: 3
PackingGroup: III
HS Code: 29310095
Mildly toxic by ingestion and inhalation. A skin and eye irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
Triethoxyvinylsilane (CAS NO.78-08-0) is also named as 4-04-00-04256 (Beilstein Handbook Reference) ; AI3-51468 ; BRN 1767229 ; CCRIS 2645 ; KBE 1003 ; NV 1107 ; Polyscience VTES ; Silane A 151 ; Silane, vinyl triethoxy 1-151 ;
Triethoxyvinylsilicane ; Union carbide A-151 ; VTES ; VTS-E ; Vinyltriethoxysilane . Triethoxyvinylsilane (CAS NO.78-08-0) is pale yellow to colorless liquid.
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