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1072-63-5

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  • 1-Vinylimidazole CAS 1072-63-5 Vinylimidazole CAS no 1072-63-5 1-Vinyl-1H-imidazole

    Cas No: 1072-63-5

  • USD $ 3.5-5.0 / Kiloliter

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1072-63-5 Usage

Chemical Properties

Brown liquid

Uses

Different sources of media describe the Uses of 1072-63-5 differently. You can refer to the following data:
1. 1-Vinylimidazole is used as a monomer in the synthesis of molecularly imprinted polymers. It is involved in the removal of vinyl protecting groups with an isoprene-catalyzed lithiation process. Also, it is involved in the preparation of magnetic-poly(divinylbenzene-1-vinylimidazole) microbeads. Further, it is used to prepare ion imprinted polyvinylimidazole-silica hybrid copolymer.
2. 1-Vinylimidazole has been employed:as functional monomer in the synthesis of molecularly imprinted polymersas monomer in the preparation of magnetic-poly(divinylbenzene-1-vinylimidazole) [m-poly(DVB-VIM)] microbeadsin the synthesis of novel ion imprinted polyvinylimidazole-silica hybrid copolymer (IIHC)in removal of the vinyl protecting group via isoprene-catalyzed lithiation process
3. Removal of the vinyl protecting group with an isoprene-catalyzed lithiation process.1

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 1072-63-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1072-63:
(6*1)+(5*0)+(4*7)+(3*2)+(2*6)+(1*3)=55
55 % 10 = 5
So 1072-63-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2/c1-2-7-4-3-6-5-7/h2-5H,1H2

1072-63-5 Well-known Company Product Price

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  • TCI America

  • (V0045)  1-Vinylimidazole  >98.0%(GC)(T)

  • 1072-63-5

  • 25mL

  • 210.00CNY

  • Detail
  • TCI America

  • (V0045)  1-Vinylimidazole  >98.0%(GC)(T)

  • 1072-63-5

  • 100mL

  • 590.00CNY

  • Detail
  • TCI America

  • (V0045)  1-Vinylimidazole  >98.0%(GC)(T)

  • 1072-63-5

  • 500mL

  • 1,690.00CNY

  • Detail
  • Alfa Aesar

  • (L16174)  1-Vinylimidazole, 99%   

  • 1072-63-5

  • 25g

  • 139.0CNY

  • Detail
  • Alfa Aesar

  • (L16174)  1-Vinylimidazole, 99%   

  • 1072-63-5

  • 100g

  • 302.0CNY

  • Detail
  • Aldrich

  • (235466)  1-Vinylimidazole  ≥99%

  • 1072-63-5

  • 235466-25G

  • 180.18CNY

  • Detail
  • Aldrich

  • (235466)  1-Vinylimidazole  ≥99%

  • 1072-63-5

  • 235466-100G

  • 388.44CNY

  • Detail

1072-63-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Vinylimidazole

1.2 Other means of identification

Product number -
Other names VINYLIMIDAZOLE,MONOMER

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1072-63-5 SDS

1072-63-5Synthetic route

2-(imidazol-1-yl)ethyl chloride
92952-84-6

2-(imidazol-1-yl)ethyl chloride

1-vinylimidazole
1072-63-5

1-vinylimidazole

Conditions
ConditionsYield
With potassium hydroxide; hydroquinone In isopropyl alcohol for 2h; Elimination; Heating;95%
1H-imidazole
288-32-4

1H-imidazole

vinyl acetate
108-05-4

vinyl acetate

1-vinylimidazole
1072-63-5

1-vinylimidazole

Conditions
ConditionsYield
With mercury(II) diacetate; hydroquinone; trifluoroacetic acid at 70℃; for 3h;71%
1H-imidazole
288-32-4

1H-imidazole

acetylene
74-86-2

acetylene

1-vinylimidazole
1072-63-5

1-vinylimidazole

Conditions
ConditionsYield
With potassium hydroxide In 1,4-dioxane70%
With copper dichloride In various solvent(s) at 180℃; under 76 - 380 Torr; for 20h;65%
copper(l) chloride In various solvent(s) for 28h; Product distribution; various time, acetylene sparging, packing diameter,;89 % Chromat.
1H-imidazole
288-32-4

1H-imidazole

Vinyl bromide
593-60-2

Vinyl bromide

1-vinylimidazole
1072-63-5

1-vinylimidazole

Conditions
ConditionsYield
With cesium fluoride In acetonitrile for 48h; Heating;66%
1H-imidazole
288-32-4

1H-imidazole

1,2-dichloro-ethane
107-06-2

1,2-dichloro-ethane

A

1-vinylimidazole
1072-63-5

1-vinylimidazole

B

1,1'-(1,2-ethanediyl)bis(imidazole)
70780-90-4

1,1'-(1,2-ethanediyl)bis(imidazole)

Conditions
ConditionsYield
Stage #1: 1H-imidazole With tetrabutylammomium bromide; potassium hydroxide at 20℃; for 1h; Inert atmosphere;
Stage #2: 1,2-dichloro-ethane at 55℃; for 48h; Inert atmosphere;
A n/a
B 65%
With potassium hydroxide; tetrabutylammomium bromide at 40℃; for 48h;A 10%
B 56%
1-(1H-imidazol-1-yl)ethyl acetate
10464-67-2

1-(1H-imidazol-1-yl)ethyl acetate

1-vinylimidazole
1072-63-5

1-vinylimidazole

Conditions
ConditionsYield
In water at 350 - 400℃;52%
1H-imidazole
288-32-4

1H-imidazole

ethylene dibromide
106-93-4

ethylene dibromide

A

1-vinylimidazole
1072-63-5

1-vinylimidazole

B

1,1'-(1,2-ethanediyl)bis(imidazole)
70780-90-4

1,1'-(1,2-ethanediyl)bis(imidazole)

Conditions
ConditionsYield
With sodium hydroxide; tetrabutylammomium bromide In toluene at 60 - 80℃; for 72h;A 10%
B 45%
1H-imidazole
288-32-4

1H-imidazole

(vinyl)trimethoxylsilane
2768-02-7

(vinyl)trimethoxylsilane

1-vinylimidazole
1072-63-5

1-vinylimidazole

Conditions
ConditionsYield
With tetrabutyl ammonium fluoride; iron(III) chloride; copper at 50℃; for 24h;41%
With tetrabutyl ammonium fluoride; copper diacetate In 1,4-dioxane; N,N-dimethyl-formamide at 30℃;38%
1-vinylimidazole
1072-63-5

1-vinylimidazole

ethyl bromide
74-96-4

ethyl bromide

3-ethyl-1-vinyl-1H-imidazol-3-ium bromide
34311-88-1

3-ethyl-1-vinyl-1H-imidazol-3-ium bromide

Conditions
ConditionsYield
at 60℃; for 3h;100%
at 40℃; for 3h; Inert atmosphere;98%
at 40℃; for 2h;97%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-bromo-hexane
111-25-1

1-bromo-hexane

1-vinyl-3-hexyl-1H-imidazol-3-ium bromide

1-vinyl-3-hexyl-1H-imidazol-3-ium bromide

Conditions
ConditionsYield
at 110℃; Continuous flow; neat (no solvent);100%
Microwave irradiation;82.6%
In tetrahydrofuran at 60℃; for 48h;51.63%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-iodo-butane
542-69-8

1-iodo-butane

1-vinyl-3-butyl-3H-imidazol-1-ium iodide
45965-87-5

1-vinyl-3-butyl-3H-imidazol-1-ium iodide

Conditions
ConditionsYield
In toluene at 110℃; for 24h;100%
for 5h; Inert atmosphere; Reflux;96%
In tert-butyl methyl ether at 20℃; for 312h;83%
In tetrahydrofuran at 20℃; for 24h;31%
Reflux;
1-vinylimidazole
1072-63-5

1-vinylimidazole

isopropyl bromide
75-26-3

isopropyl bromide

1-vinyl-3-isopropylimidazolium bromide
1020109-60-7

1-vinyl-3-isopropylimidazolium bromide

Conditions
ConditionsYield
for 16h; Reflux;100%
1-vinylimidazole
1072-63-5

1-vinylimidazole

2-acrylamido-2-methylpropanesulfonic acid
15214-89-8

2-acrylamido-2-methylpropanesulfonic acid

C7H13NO4S*C5H6N2
942205-52-9

C7H13NO4S*C5H6N2

Conditions
ConditionsYield
In methanol at 20℃; for 4h;100%
1-vinylimidazole
1072-63-5

1-vinylimidazole

hydrogen
1333-74-0

hydrogen

N-Ethylimidazole
7098-07-9

N-Ethylimidazole

Conditions
ConditionsYield
With C61H98ClN3P2Ru In dichloromethane-d2 at 50℃; under 3040.2 Torr; for 10h; Reagent/catalyst; Time;100%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1,2,3,4,5,6-hexa(bromomethyl)benzene
3095-73-6

1,2,3,4,5,6-hexa(bromomethyl)benzene

C42H48N12(6+)*6Br(1-)

C42H48N12(6+)*6Br(1-)

Conditions
ConditionsYield
In tetrahydrofuran at 60℃; Inert atmosphere;100%
In acetonitrile at 80℃; for 48h; Inert atmosphere;82%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1,2,4,5-tetrabromomethylbenzene
15442-91-8

1,2,4,5-tetrabromomethylbenzene

1,2,4,5-tetrakis (1’-methylene-3’-vinylimidazolium bromide)benzene

1,2,4,5-tetrakis (1’-methylene-3’-vinylimidazolium bromide)benzene

Conditions
ConditionsYield
In tetrahydrofuran at 60℃; Inert atmosphere;100%
With 2,6-di-tert-butyl-4-methyl-phenol In acetonitrile at 64.84℃; for 72h;
1-vinylimidazole
1072-63-5

1-vinylimidazole

1,3,5-Tris(bromomethyl)benzene
18226-42-1

1,3,5-Tris(bromomethyl)benzene

1,3,5-tris(1’-methylene-3’-vinylimidazolium bromide)benzene

1,3,5-tris(1’-methylene-3’-vinylimidazolium bromide)benzene

Conditions
ConditionsYield
In tetrahydrofuran at 60℃; Inert atmosphere;100%
With 2,6-di-tert-butyl-4-methyl-phenol In acetonitrile at 64.84℃; for 72h;
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-dodecylbromide
143-15-7

1-dodecylbromide

1-vinyl-3-dodecyl-3H-imidazol-1-ium bromide

1-vinyl-3-dodecyl-3H-imidazol-1-ium bromide

Conditions
ConditionsYield
for 5h; Inert atmosphere; Reflux;99%
In methanol at 100℃; for 10h;96%
In methanol at 100℃; for 10h; Temperature;96%
1-vinylimidazole
1072-63-5

1-vinylimidazole

n-iodooctadecane
629-93-6

n-iodooctadecane

1-vinyl-3-octadecyl-3H-imidazol-1-ium iodide
1276122-97-4

1-vinyl-3-octadecyl-3H-imidazol-1-ium iodide

Conditions
ConditionsYield
for 5h; Inert atmosphere; Reflux;99%
In acetone at 100℃; for 12h; Autoclave; High pressure;
1-vinylimidazole
1072-63-5

1-vinylimidazole

benzyl bromide
100-39-0

benzyl bromide

3-benzyl-1-vinyl-1H-imidazol-3-ium bromide
67691-05-8

3-benzyl-1-vinyl-1H-imidazol-3-ium bromide

Conditions
ConditionsYield
In acetonitrile at 100℃; for 24h; Inert atmosphere;99%
In acetonitrile at 88℃; for 12h;94%
In tetrahydrofuran at 20℃; for 24h;26%
In methanol at 50℃; for 12h;
In tetrahydrofuran at 40℃; for 24h; Inert atmosphere;
1-vinylimidazole
1072-63-5

1-vinylimidazole

trifluoromethanesulfonic acid ethyl ester
425-75-2

trifluoromethanesulfonic acid ethyl ester

3-ethyl-1-vinylimidazolium triflate
932031-92-0

3-ethyl-1-vinylimidazolium triflate

Conditions
ConditionsYield
In dichloromethane at 0℃; for 2h; Inert atmosphere;99%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-bromomethyl-4-nitro-benzene
100-11-8

1-bromomethyl-4-nitro-benzene

1-ethenyl-3-[(4-nitrophenyl)methyl]-1H-imidazol-3-ium bromide

1-ethenyl-3-[(4-nitrophenyl)methyl]-1H-imidazol-3-ium bromide

Conditions
ConditionsYield
In ethyl acetate for 24h; Reflux; Inert atmosphere;99%
1-vinylimidazole
1072-63-5

1-vinylimidazole

(bromomethyl)pentafluorobenzene
1765-40-8

(bromomethyl)pentafluorobenzene

3-(2,3,4,5,6-pentafluorobenzyl)-1-vinylimidazol-1-ium bromide

3-(2,3,4,5,6-pentafluorobenzyl)-1-vinylimidazol-1-ium bromide

Conditions
ConditionsYield
In acetonitrile at 20℃; for 48h; Cooling with ice; Inert atmosphere;99%
In acetonitrile at 88℃; for 12h;91%
1-vinylimidazole
1072-63-5

1-vinylimidazole

5,10,15,20-tetraphenyl porphyrin iron
16591-56-3

5,10,15,20-tetraphenyl porphyrin iron

bis(1-vinylimidazole)(meso-tetraphenylporphyrinato)iron(II)
125227-66-9

bis(1-vinylimidazole)(meso-tetraphenylporphyrinato)iron(II)

Conditions
ConditionsYield
In dichloromethane under Ar, soln. mixture, stirred, warmed slightly, 10 min; filtration, filtrate layered with hexane, crystn. (-16°C, 3 d);98.4%
1-vinylimidazole
1072-63-5

1-vinylimidazole

benzyl chloride
100-44-7

benzyl chloride

1-benzyl-3-vinylimidazolium chloride

1-benzyl-3-vinylimidazolium chloride

Conditions
ConditionsYield
In acetonitrile at 70℃; for 24h;98.17%
1-vinylimidazole
1072-63-5

1-vinylimidazole

allyl bromide
106-95-6

allyl bromide

1-allyl-3-vinyl-imidazolium bromide

1-allyl-3-vinyl-imidazolium bromide

Conditions
ConditionsYield
In acetonitrile at 100℃; for 24h; Inert atmosphere;98%
at 65℃; for 12h;
In neat (no solvent) at 79.84℃; for 24h;
at 60℃; for 3h;
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-Bromooctadecane
112-89-0

1-Bromooctadecane

1-vinyl-3-octadecyl-3H-imidazol-1-ium bromide

1-vinyl-3-octadecyl-3H-imidazol-1-ium bromide

Conditions
ConditionsYield
for 5h; Inert atmosphere; Reflux;98%
In acetonitrile at 60℃; for 72h;96.5%
In acetonitrile at 60℃; for 72h;96.5%
1-vinylimidazole
1072-63-5

1-vinylimidazole

bis(2-phenethyl)phosphine
93017-30-2

bis(2-phenethyl)phosphine

bis(2-phenethyl)-[2-(1H-imidazolyl)ethyl]phosphane
1289679-11-3

bis(2-phenethyl)-[2-(1H-imidazolyl)ethyl]phosphane

Conditions
ConditionsYield
With 2,2'-azobis(isobutyronitrile) In 1,4-dioxane at 65 - 70℃; for 6h; Inert atmosphere;98%
1-vinylimidazole
1072-63-5

1-vinylimidazole

bis(2-phenylethyl)phosphine selenide
923023-81-8

bis(2-phenylethyl)phosphine selenide

[2-(1H-imidazol-1-yl)ethyl]diphenethylphosphine selenide
1319805-22-5

[2-(1H-imidazol-1-yl)ethyl]diphenethylphosphine selenide

Conditions
ConditionsYield
In 1,4-dioxane for 1.5h; UV-irradiation; Inert atmosphere; regioselective reaction;98%
1-vinylimidazole
1072-63-5

1-vinylimidazole

bis(2-phenylethyl)phosphane sulfide

bis(2-phenylethyl)phosphane sulfide

[2-(1H-imidazol-1-yl)ethyl]diphenethylphosphine sulfide
1319805-19-0

[2-(1H-imidazol-1-yl)ethyl]diphenethylphosphine sulfide

Conditions
ConditionsYield
In 1,4-dioxane for 2h; UV-irradiation; Inert atmosphere; regioselective reaction;98%
In neat (no solvent) at 80℃; for 10h; Inert atmosphere; regioselective reaction;93%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-Iodododecane
4292-19-7

1-Iodododecane

1-vinyl-3-dodecyl-3H-imidazol-1-ium iodide
38862-37-2

1-vinyl-3-dodecyl-3H-imidazol-1-ium iodide

Conditions
ConditionsYield
for 5h; Inert atmosphere; Reflux;98%
In ethyl acetate for 24h; Reflux; Inert atmosphere;97%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-Bromotetradecane
112-71-0

1-Bromotetradecane

1-vinyl-3-tetradecyl-3H-imidazol-1-ium bromide
888500-15-0

1-vinyl-3-tetradecyl-3H-imidazol-1-ium bromide

Conditions
ConditionsYield
for 5h; Inert atmosphere; Reflux;98%
In ethyl acetate for 24h; Reflux; Inert atmosphere;95%
In methanol at 60℃; for 15h;
In acetonitrile Reflux;
1-vinylimidazole
1072-63-5

1-vinylimidazole

1,4-dibromo-butane
110-52-1

1,4-dibromo-butane

1,4-butanediyl-3,3’-bis-1-vinylimidazolium dibromide

1,4-butanediyl-3,3’-bis-1-vinylimidazolium dibromide

Conditions
ConditionsYield
In chloroform for 24h; Reflux;98%
In acetonitrile at 60℃; for 24h;96%
Stage #1: 1-vinylimidazole; 1,4-dibromo-butane In tetrahydrofuran at 20℃; for 1h;
Stage #2: In tetrahydrofuran at 100℃; Autoclave; High pressure;
91%
1-vinylimidazole
1072-63-5

1-vinylimidazole

trimethyl orthoformate
149-73-5

trimethyl orthoformate

1-ethenyl-3-methyl-1H-imidazolium hexafluorophosphate

1-ethenyl-3-methyl-1H-imidazolium hexafluorophosphate

Conditions
ConditionsYield
With ammonium hexafluorophosphate Schlenk technique; Reflux;98%
With ammonium hexafluorophosphate at 110℃; for 22h; Inert atmosphere;97%
1-vinylimidazole
1072-63-5

1-vinylimidazole

1,4-butane sultone
1633-83-6

1,4-butane sultone

1-(butyl-4-sulfonate)-3-vinylimidazolium

1-(butyl-4-sulfonate)-3-vinylimidazolium

Conditions
ConditionsYield
at 70℃; for 10h; Inert atmosphere;98%
In acetonitrile at 0 - 85℃; for 72h;63%
In acetonitrile at 85℃; for 120h; Inert atmosphere;
In toluene at 60℃; for 24h;
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-iodo-propane
107-08-4

1-iodo-propane

1-vinyl-3-propylimidazolium iodide
38862-36-1

1-vinyl-3-propylimidazolium iodide

Conditions
ConditionsYield
With Irganox at 60℃; for 20h; Inert atmosphere;97%
In tert-butyl methyl ether at 20℃; for 48h;44%
1-vinylimidazole
1072-63-5

1-vinylimidazole

bromoacetic acid
79-08-3

bromoacetic acid

1-carboxymethyl-3-vinylimidazolium bromide
1276015-40-7

1-carboxymethyl-3-vinylimidazolium bromide

Conditions
ConditionsYield
In acetone at 20℃; for 24h;97%
In toluene for 24h; Inert atmosphere; Reflux;90%
at 60℃; for 12h; Inert atmosphere;
In acetonitrile at 60℃; for 12h; Schlenk technique; Inert atmosphere;
1-vinylimidazole
1072-63-5

1-vinylimidazole

1-iodohexadecane
544-77-4

1-iodohexadecane

1-vinyl-3-hexadecyl-3H-imidazol-1-ium iodide
38862-38-3

1-vinyl-3-hexadecyl-3H-imidazol-1-ium iodide

Conditions
ConditionsYield
for 5h; Inert atmosphere; Reflux;97%
In acetone at 100℃; for 12h; Autoclave; High pressure;

1072-63-5Relevant articles and documents

Highly Recoverable Pd(II) Catalysts for the Mizoroki-Heck Reaction Based on N-Heterocyclic Carbenes and Poly(benzyl ether) Dendrons

Ortiz, Alba,Gómez-Sal, Pilar,Flores, Juan C.,De Jesús, Ernesto

, p. 3598 - 3610 (2018)

Two series of bis(imidazolylidene)palladium complexes of general formula [PdBr2(NHC)2] have been prepared. The molecular weight of the complexes was enlarged by bonding poly(benzyl ether) dendrons of increasing size (G0 to G3) at the nitrogen atom of the NHC ligands. Complexes 1-4 contain monodentate NHC ligands coordinated in a trans mode, whereas complexes 9-12 contain a chelating ethylene-bridged bis(NHC) ligand. The complexes were recovered from the product stream of a Mizoroki-Heck reaction by nanofiltration through thermally and chemically stable ceramic membranes. The recoverability is better for larger complexes and chelate ligands. In particular, chelate G3 complex 12 maintained a constant activity during the 13 recovery cycles performed, affording an accumulated turnover number (TON) of 13a€000. On average, around 99.5% of the metal is recovered in each recovery cycle, and contamination by palladium is only 3 mg per kg of product. Several models to explain the efficiency of the recovery are discussed.

Solvent-free copper/iron co-catalyzed N-arylation reactions of nitrogen-containing heterocycles with trimethoxysilanes in air

Song, Ren-Jie,Deng, Chen-Liang,Xie, Ye-Xiang,Li, Jin-Heng

, p. 7845 - 7848 (2007)

A solvent-free copper/iron-catalyzed N-arylation of nitrogen-containing heterocycles with trimethoxysilanes method for the formation of C-N bonds has been developed. In the presence of Cu, FeCl3, TBAF, and air, a variety of nitrogen-containing heterocycles including imidazoles and triazoles were coupled with aryltrimethoxysilanes and vinyltrimethoxysilane to afford the corresponding products in moderate to excellent yields. It is noteworthy that the reaction is conducted under solvent-free and relatively low Cu/FeCl3 loadings conditions.

-

Shostakovskii,et al.

, (1969)

-

Direct N- and C-vinylation with trimethoxyvinylsilane

Arsenyan, Pavel,Petrenko, Alla,Paegle, Edgars,Belyakov, Sergey

experimental part, p. 326 - 328 (2012/02/04)

Treatment of nucleobases, nucleosides, 5-membered N-heterocycles and terminal alkynes with trimethoxyvinylsilane in the presence of copper(II) acetate-TBAF system as catalyst affords the vinylation products.

METHOD OF PREPARING FLUORINATED ALKOXYTRIALKYLSILANES

-

Page/Page column 11-12, (2008/06/13)

The present invention relates to a process for preparing alkoxytrialkylsilane, and in particular to a process, wherein an imidazole compound is added as a HCl scavenger and a reaction promoter, thereby enhancing the yield of fluorinated alkoxytrialkylsilanes and reducing corrosion problem.

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