DayangChem exported this product to many countries and regions at best price. If you are looking for the material's manufacturer or supplier in China, DayangChem is your best choice. Pls contact with us freely for getting detailed product spe
Cas:75-94-5
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Cas:75-94-5
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inquiryTIANFUCHEM--75-94-5--Trichlorovinylsilane in stock Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business relation
Cas:75-94-5
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inquiryChemical Name: Vinyltrichlorosilane Formula: CH2=CHSiCl3 Appearance: Vinyltrichlorosilane is Colorless to light-yellow liquid. Soluble in most organic solvents. Prone to hydrolysis and alcoholysis. Applications: Applied as an important
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
Product Detail Minimum Order Qty. 10 Gram
Cas:75-94-5
Min.Order:10 Gram
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Type:Trading Company
inquiryEnglish name: Trichlorovinylsilane CAS RN: 75-94-5 EINECS No.: 200-917-8 Molecular formula: C2H3Cl3Si Appearance: Colorless and transparent liquid Density( g/cm3):1.270 ± 0.0050 Refractive index: 1.436 ± 0.0050 Boiling point:
Cas:75-94-5
Min.Order:1 Kilogram
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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Min.Order:4 Kilogram
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This product is an important raw material for the synthesis of a variety of other vinyl silicone coupling agents Appearance:colorless transparent liquid Storage:Store in a cool, dry, well ventilated warehouse. Package:240kg iron drum or 1200kg IBC
Cas:75-94-5
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
Product Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:75-94-5
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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Min.Order:1 Kilogram
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Min.Order:10 Milligram
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Type:Lab/Research institutions
inquiryWD Silicone (formerly Wuhan University Chemical Plant founded in 1958) is one of the earliest plants in China to produce organosilicone products. Since the reform in 2000, WD Silicone has become a major manufacturer of silane coupling agents in
Trichlorovinylsilane Basic information Product Name: Trichlorovinylsilane
Cas:75-94-5
Min.Order:100 Gram
Negotiable
Type:Trading Company
inquiryWhy Choose Us: 1.Own chemical factory 2.Abundant professional production experience 3.Sample is free of charge and in stock with fast delivery 4.Price,quality&service,we care that all your cares 5.Prompt reply keep in touch to sa
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Min.Order:1 Kilogram
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Type:Trading Company
inquiryChangzhou Extraordinary Pharmatech co., LTD. As a leading chemical manufacturer and supplier in China.DAS authentication is passed.We can provide the popular precursor chemicals, we have our own strong R & D team, have our own laboratories and fa
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Cas:75-94-5
Min.Order:1 Kilogram
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Type:Other
inquiryConditions | Yield |
---|---|
With (η6-toluene)Ni(SiCl3)2 for 42h; Mechanism; Product distribution; Ambient temperature; | A 23% B 14% C 98% D n/a |
Conditions | Yield |
---|---|
With tris(triphenylphosphine)ruthenium(II) chloride; trichlorosilane In xylene at 80℃; for 3h; | 90% |
With {Rh(μ-Cl)(CO)(eta.2-cyclooctene)}2; trichlorosilane at 40℃; for 4h; | 12% |
With aluminum oxide; palladium/alumina; trichlorosilane |
tetravinylsilane
A
dichlorodivinylsilane
B
trichlorovinylsilane
C
chlorotrivinylsilane
Conditions | Yield |
---|---|
With hydrogenchloride; iron(III) chloride at 24 - 52℃; Product distribution; oth. catalysts; | A 13.8% B 0.5% C 88% |
chlorotrivinylsilane
A
(n-pr-2-Cl)SiCl3
B
dichlorodivinylsilane
C
trichlorovinylsilane
Conditions | Yield |
---|---|
With hydrogenchloride; iron(III) chloride at 24 - 52℃; Product distribution; | A 4% B 73% C 16% |
Conditions | Yield |
---|---|
With trichlorosilane; dichlorotetraammine platinum; silica gel In various solvent(s) at 150℃; under 712.557 Torr; | A 72% B n/a |
With di(rhodium)tetracarbonyl dichloride; trichlorosilane at 20℃; for 2h; Yields of byproduct given; | A 19.0 % Chromat. B n/a |
With magnesium hydrosilicate; trichlorosilane; platinum |
Conditions | Yield |
---|---|
With hydrogenchloride; iron(III) chloride at 24 - 52℃; Product distribution; | A 19.5% B 69% |
Conditions | Yield |
---|---|
With ferrosilicon | |
With copper | |
With quinoline In quinoline boiling of (CH2ClCH2)SiCl3 with quinoline;; | |
With quinoline In quinoline boiling of (CH2ClCH2)SiCl3 with quinoline;; |
phenylacetylene
A
trichlorovinylsilane
B
(E)-1-phenyl-2-trichlorosilylethene
Conditions | Yield |
---|---|
With trichlorosilane; TB*2RhCl3 for 24h; Ambient temperature; Title compound not separated from byproducts; | A 95 % Spectr. B 5 % Spectr. |
With trichlorosilane; TB*2RhCl3 for 24h; Ambient temperature; | A 95 % Spectr. B 5 % Spectr. |
trichlorosilane
acetylene
A
trichlorovinylsilane
B
1,2-bis(trichlorosilyl)ethane
Conditions | Yield |
---|---|
at 260 - 300℃; |
trichlorosilane
acetylene
A
trichlorovinylsilane
B
1,2-bis(trichlorosilyl)ethane
Conditions | Yield |
---|---|
at 150 - 250℃; under 12503.6 - 18387.7 Torr; |
sulfuryl dichloride
diethyldichlorosilane
dibenzoyl peroxide
A
dichlorodivinylsilane
B
trichlorovinylsilane
Conditions | Yield |
---|---|
Erhitzen des Reaktionsprodukts mit Chinolin auf 230grad; |
sulfuryl dichloride
ethyltrichlorosilane
dibenzoyl peroxide
trichlorovinylsilane
Conditions | Yield |
---|---|
Erhitzen des Reaktionsprodukts in Chinolin auf 200-230grad; |
quinoline
Trichloro-(1-chloro-ethyl)-silane
A
tetrachlorosilane
B
trichlorovinylsilane
aluminium trichloride
Trichloro-(1-chloro-ethyl)-silane
A
tetrachlorosilane
B
trichlorovinylsilane
Trichloro-(1-chloro-ethyl)-silane
A
tetrachlorosilane
B
ethene
C
trichlorovinylsilane
Conditions | Yield |
---|---|
under 610 Torr; Pyrolysis; |
Conditions | Yield |
---|---|
at 350 - 400℃; |
1,1-dichloroethane
A
trichlorovinylsilane
B
1,2-bis(trichlorosilyl)ethane
C
1,1-bis-dichlorosilanyl-ethane
D
1,1-Bis(trichlorosilyl)ethane
Conditions | Yield |
---|---|
at 360 - 380℃; weitere Produkten: Dichlor-vinyl-silan; 1-Dichlorsilyl-1-trichlorsilyl-aethan; |
Conditions | Yield |
---|---|
With trichlorosilane at 426.9℃; Equilibrium constant; Thermodynamic data; E(excit.), ΔH, other temp.; |
chloroethylene
silicon
A
dichlorovinylsilane
B
dichlorodivinylsilane
C
trichlorovinylsilane
Conditions | Yield |
---|---|
tin In neat (no solvent) Si-Sn and CH2CHCl at 400°C;; mixt. obtained;; |
trichlorosilane
acetylene
A
trichlorovinylsilane
B
1,2-bis(trichlorosilyl)ethane
Conditions | Yield |
---|---|
platinum In neat (no solvent) HSiCl3 and acetylene with platinized asbestos as catalyst at 175°C under pressure;; | |
platinum In neat (no solvent) HSiCl3 and acetylene with platinized asbestos as catalyst at 175°C under pressure;; | |
platinum In neat (no solvent) HSiCl3 and acetylene with platinized asbestos as catalyst at 175°C under pressure;; |
trichlorovinylsilane
1,3,5,7,11,13,15-octakis[2-(trichlorosilyl)ethyl]pentacyclo[9.5.1.13,9.15,15.17,13]octasiloxane
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate; 2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosan-1,3,5,7,9,11,13,15-octanol In isopropyl alcohol for 22h; Heating; | 100% |
Conditions | Yield |
---|---|
With benzophenone for 4h; Inert atmosphere; UV-irradiation; | 100% |
trichlorovinylsilane
tetrakis(2-sulfanylethyl) silicate
Conditions | Yield |
---|---|
With benzophenone In diethyl ether for 4h; Inert atmosphere; UV-irradiation; | 100% |
lauric acid
trichlorovinylsilane
Octanoic acid
n-tetradecanoic acid
C36H68O6Si
Conditions | Yield |
---|---|
In toluene at 60 - 150℃; for 4h; | 99.82% |
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% |
[(cyclopentadienyl)Co(trimethylvinylsilane)2]
trichlorovinylsilane
[(cyclopentadienyl)Co(trichlorovinylsilane)2]
Conditions | Yield |
---|---|
In diethyl ether byproducts: (CH3)3SiCHCH2; (Ar), Schlenk techniques; dropwise addn. of Si compd. to soln. of Co complex in Et2O at -30°C over 2 min, stirring for 5 min; evapn. under reduced pressure at -20°C, drying under vacuum; | 99% |
Conditions | Yield |
---|---|
With N-benzyl-N,N,N-triethylammonium chloride Substitution; | 98% |
Conditions | Yield |
---|---|
With iron(III) chloride at 85℃; for 0.0166667h; polycondensation; | 98% |
Conditions | Yield |
---|---|
With iron(III) chloride at 85℃; polycondensation; | 98% |
trichlorovinylsilane
monochloroborane dimethyl sulfide complex
Conditions | Yield |
---|---|
In toluene byproducts: dimethylsulfide; in Ar atmosphere into precooled toluene soln. of trichlorovinylsilane chloroborane-dimethylsulfide in toluene added dropwise at 10 °C for6 h; stirred at room temp. 20 h; dimethylsulfide and toluene removed at 0.02 Torr at 60 °C; elem. anal.; | 98% |
Conditions | Yield |
---|---|
With trichlorosilane | 97% |
With trichlorosilane; platinum on activated charcoal for 12h; Ambient temperature; | 92% |
With dihydrogen hexachloroplatinate; trichlorosilane at 130℃; for 2.5h; Inert atmosphere; | 72% |
Conditions | Yield |
---|---|
With benzophenone for 10h; Inert atmosphere; UV-irradiation; | 97% |
(heating); |
Conditions | Yield |
---|---|
With benzophenone for 4h; Inert atmosphere; UV-irradiation; | 97% |
Conditions | Yield |
---|---|
With tetrachlorosilane In water at 0℃; for 1h; Concentration; Reflux; Large scale; | 96.1% |
Conditions | Yield |
---|---|
With (η6-toluene)Ni(SiCl3)2 for 42h; Mechanism; Product distribution; Ambient temperature; | A 23% B 14% C 98% D n/a |
Conditions | Yield |
---|---|
With {palladium-dichloro-(P(C3H7)3)2}; trichlorosilane In xylene at 80℃; for 3h; | A 63% B 12% |
With bis(tributylphosphine)dichloropalladium(II); trichlorosilane In xylene at 80℃; for 3h; | A 22% B 63% |
chloroethylene
A
1,1-Dichloro-2,5-dihydro-1H-silole
B
trichlorovinylsilane
C
1,2-bis(trichlorosilyl)ethene
D
Phenyltrichlorosilane
E
1,1,3,3-tetrachloro-1,3-disilacyclohex-4-ene
Conditions | Yield |
---|---|
With hexachlorodisilane at 500℃; for 0.00694444h; Product distribution; Mechanism; other temperature 550 deg C; | A 1.52% B 55.7% C 3.91% D 1.06% E 7.07% F n/a |
Conditions | Yield |
---|---|
at 150℃; | 52% |
dihydrogen hexachloroplatinate In ethanol at 125℃; under 1535.79 Torr; Product distribution / selectivity; Inert atmosphere; | |
platinum In neat (no solvent) HSiCl3 and C2H2 at 130°C with Pt on coal (catalyst);; | |
platinum In neat (no solvent) HSiCl3 and C2H2 at 175°C with platinized asbestos as catalyst;; | |
In neat (no solvent) byproducts: Cl3SiCH2CH2SiCl3; passing HSiCl3 and C2H2 through a tube at 610°C;; |
Conditions | Yield |
---|---|
at 810℃; Product distribution; vacuum flash pyrolysis; | A n/a B 46% |
chloroethylene
Phenyltrichlorosilane
A
trichlorovinylsilane
B
chlorobenzene
C
benzene
Conditions | Yield |
---|---|
at 630℃; Product distribution; gas phase reaction, quartz tube, contact time 30 sec; | A 3% B 2% C 34% |
chloroethylene
1-chloro-2-trichlorosilylethylene
A
trichlorovinylsilane
B
1,2-bis(trichlorosilyl)ethene
C
trichlorosilylacetylene
Conditions | Yield |
---|---|
at 560℃; Product distribution; gas phase reaction, quartz tube, contact time 30 sec; | A 6.7% B 1.7% C 18.7% |
Conditions | Yield |
---|---|
With sulfuryl dichloride; dibenzoyl peroxide Erhitzen des Reaktionsprodukts mit Chinolin bis auf 200-230grad; |
Conditions | Yield |
---|---|
With copper; silicon at 300 - 350℃; |
Conditions | Yield |
---|---|
With copper; silicon at 300 - 350℃; | |
With silicon; copper | |
With Si-Cu In neat (no solvent) Si-Cu (9:1) and CH2CHCl at 300-350°C;; |
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% |
dimethylmonochlorosilane
trichlorovinylsilane
1-(Chloro-dimethyl-silanyl)-2-trichlorosilanyl-ethane
Conditions | Yield |
---|---|
chloroplatinic acid 1,1,3,3-tetramethyl-1,3-divinyldisiloxane complex at 40℃; for 6h; | 95% |
Conditions | Yield |
---|---|
carbonylchlorohydridobis(tricyclohexylphosphine)ruthenium(II) In dichloromethane at 40℃; for 3h; | 95% |
trichlorovinylsilane
potassium tert-butylate
tris(tert-butoxy)(vinyl)silane
Conditions | Yield |
---|---|
In hexane at 20℃; for 24h; | 95% |
Conditions | Yield |
---|---|
With tetrachlorosilane In water at 0℃; for 4h; pH=6; Concentration; Reflux; Large scale; | 94.8% |
Conditions | Yield |
---|---|
In dichloromethane at 50 - 80℃; for 3h; | A 93.2% B 5.2% |
hydroxymethyl tert-butyl peroxide
trichlorovinylsilane
Conditions | Yield |
---|---|
With triethylamine at -5℃; | 93% |
trichlorovinylsilane
1,3-diallyl-4-(trimethylsilyloxy)-2,6-dioxo-1,3,5-triazine
Conditions | Yield |
---|---|
at 120 - 160℃; | 93% |
ethyl 2-hydroxypropionate
trichlorovinylsilane
vinyltris(ethyl lactato)silane
Conditions | Yield |
---|---|
With triethylamine In toluene at 20℃; for 3h; | 93% |
Conditions | Yield |
---|---|
at 20℃; for 24h; | 93% |
Conditions | Yield |
---|---|
With triethylamine In toluene at 20℃; Inert atmosphere; | 93% |
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% |
trichlorovinylsilane
Dimethylphenylsilane
A
Dichloromethylvinylsilane
B
1,2-bis(trichlorosilyl)ethane
C
Si,Si,Si-trichloro-Si',Si'-dimethyl-Si'-phenyl-Si,Si'-ethanediyl-bis-silane
D
Phenyltrichlorosilane
Conditions | Yield |
---|---|
With dihydrogen hexachloroplatinate Product distribution; Mechanism; Heating; determination of side products; | A 0.7% B 3.5% C 92.3% D 0.9% |
Conditions | Yield |
---|---|
With hydrogen; nickel for 6h; | 92% |
Conditions | Yield |
---|---|
[Cl2(PCy3)(IMesH2)Ru(=CHPh)] In dichloromethane for 1h; Heating; | 92% |
[Cl2(PCy3)(IMesH2)Ru(=CHPh)] In dichloromethane for 1h; Heating; |
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