TRIMETHOXYCHLOROSILANEDISC 05/06/04
- CasNo:4668-00-2
Product Description
Chinese Manufacturer Supply TRIMETHOXYCHLOROSILANEDISC 05/06/04 4668-00-2 On Stock with Competitive Price
- Molecular Formula: C3H9 Cl O3 Si
- Molecular Weight: 156.641
- Vapor Pressure: 114mmHg at 25°C
- Refractive Index: 1.35
- Boiling Point: 75.7°C at 760 mmHg
- Flash Point: 2.2°C
- PSA： 27.69000
- Density: 1.085g/cm3
- LogP: 0.60000
TRIMETHOXYCHLOROSILANEDISC 05/06/04(Cas 4668-00-2) Usage
|
General Description |
TRIMETHOXYCHLOROSILANEDISC 05/06/04 is a chemical compound used in the manufacturing of silicones and silanes. It is a colorless, flammable liquid that is highly reactive with water. TRIMETHOXYCHLOROSILANEDISC 05/06/04 is commonly used as a coupling agent, adhesion promoter, and surface modifier, particularly in the production of adhesives, sealants, and coatings. It has the ability to bond to both organic and inorganic surfaces, making it useful in a variety of industrial applications. However, it is also highly corrosive and can cause severe skin and eye irritation, as well as respiratory issues if inhaled. Therefore, proper handling and safety precautions are necessary when working with TRIMETHOXYCHLOROSILANEDISC 05/06/04. |
InChI:InChI=1/C3H9ClO3Si/c1-5-8(4,6-2)7-3/h1-3H3
4668-00-2 Relevant articles
Stable silanetriols that contain tert-alkoxy groups: Versatile precursors of siloxane-based nanomaterials
Suzuki, Jumpei,Shimojima, Atsushi,Fujimoto, Yasuhiro,Kuroda, Kazuyuki
, p. 973 - 980 (2008)
Novel tert-alkoxysilanetriols (ROSi(OH)3...
Hierarchically porous monolithic silica with varying porosity using bis(trimethoxysilyl)arenes as precursors
Von Der Lehr, Martin,Ellinghaus, Rüdiger,Smarsly, Bernd M.
, p. 4455 - 4463 (2016)
The ortho-, meta- and para-isomers of bi...
Molecularly designed nanoparticles by dispersion of self-assembled organosiloxane-based mesophases
Sakamoto, Shigeru,Tamura, Yasuhiro,Hata, Hideo,Shimojima, Atsushi,Kuroda, Kazuyuki,Sakamoto, Yasuhiro
, p. 9173 - 9177,5 (2014)
The design of siloxane-based nanoparticl...
-
Murata
, p. 347 (1952)
-
ORGANOMETALLIC COMPOUND AND METHOD
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Page/Page column 9; 10, (2017/09/05)
A class of organometallic compounds is p...
FLUORINE-CONTAINING SILOXANE COMPOUND, METHOD FOR PRODUCING THE SAME, COATING AGENT COMPRISING THE SAME, AND SURFACE TREATMENT METHOD FOR GLASS BASE MATERIAL
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Paragraph 0067-0069, (2017/09/21)
PROBLEM TO BE SOLVED: To provide a fluor...
4668-00-2 Process route
-
-
2487-90-3
trimethoxysilane
-
-
563-47-3
3-Chloro-2-methylpropene
-
-
754992-03-5
3-chloroisobutylchlorodimethoxysilane
-
-
bis(trimethoxysilyl)isobutane
-
-
4668-00-2
chlorotrimethoxysilane
-
-
681-84-5
tetramethylorthosilicate
-
-
18395-30-7
isobutyltrimethoxysilane
-
-
17256-27-8
3-chloro-2-methylpropyltrimethoxysilane
-
-
513-36-0
isobutyryl chloride
| Conditions | Yield |
|---|---|
|
ruthenium trichloride;
In
methanol;
at 20 - 83 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
With
1,1'-(1,2-ethanediyl)bisbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 83 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
trimethoxysilane;
With
1,1'-(1,2-ethanediyl)bisbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-Chloro-2-methylpropene;
at 78 - 83 ℃;
for 2h;
|
|
|
trimethoxysilane;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-Chloro-2-methylpropene;
at 78 - 83 ℃;
for 2h;
|
-
-
2487-90-3
trimethoxysilane
-
-
107-05-1
3-chloroprop-1-ene
-
-
bis(trimethoxysilyl)propane
-
-
253586-30-0
3-chloropropyltrichlorosilane
-
-
4668-00-2
chlorotrimethoxysilane
-
-
681-84-5
tetramethylorthosilicate
-
-
540-54-5
1-Chloropropane
-
-
1067-25-0
n-propyltrimethoxysilane
-
-
2530-87-2
3-Chloropropyltrimethoxysilan
| Conditions | Yield |
|---|---|
|
With
toluene;
ruthenium trichloride;
In
methanol;
at 20 - 83 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
[ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2;
In
dichloromethane;
at 20 - 83 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
ruthenium trichloride;
In
methanol;
at 75 - 169 ℃;
for 18h;
Product distribution / selectivity;
Continuous operation;
|
|
|
ruthenium trichloride;
In
methanol;
at 20 - 81 ℃;
for 2 - 10h;
Product distribution / selectivity;
Batch type operation;
|
|
|
With
Therminol59;
ruthenium trichloride;
In
methanol;
at 20 - 83 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
With
1-butylbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 81 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
With
methoxybenzene;
ruthenium trichloride;
In
methanol;
at 20 - 81 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
With
triphenylmethane;
ruthenium trichloride;
In
methanol;
at 20 - 81 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
With
ethylbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 81 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
With
1,1'-(1,2-ethanediyl)bisbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 96 ℃;
for 2h;
Product distribution / selectivity;
|
|
|
With
Diphenylmethane;
ruthenium trichloride;
In
methanol;
at 75 - 169 ℃;
for 18h;
Product distribution / selectivity;
Continuous operation;
|
|
|
With
Diphenylmethane;
ruthenium trichloride;
In
methanol;
at 20 - 81 ℃;
for 2 - 10h;
Product distribution / selectivity;
Batch type operation;
|
|
|
trimethoxysilane;
ruthenium trichloride;
In
methanol; toluene;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 78 - 83 ℃;
for 2h;
|
|
|
trimethoxysilane; 3-chloroprop-1-ene;
at 75 - 169 ℃;
for 18h;
Heating / reflux;
3-chloroprop-1-ene;
at 79 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
ruthenium trichloride;
In
methanol; toluene;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 79 - 82 ℃;
for 2h;
|
|
|
trimethoxysilane;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 20 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
[RuCl2(p-cymene)]2;
In
dichloromethane;
at 20 - 78 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 78 - 83 ℃;
for 2h;
|
|
|
trimethoxysilane;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 79 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
With
1-butylbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 80 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
With
methoxybenzene;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 80 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
With
triphenylmethane;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 80 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
With
ethylbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 80 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
With
1,1'-(1,2-ethanediyl)bisbenzene;
ruthenium trichloride;
In
methanol;
at 20 - 95 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 60 - 96 ℃;
for 2h;
|
|
|
trimethoxysilane;
With
Diphenylmethane;
ruthenium trichloride;
In
methanol;
at 20 - 80 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 80 - 81 ℃;
for 2h;
|
|
|
trimethoxysilane;
With
therminol;
ruthenium trichloride;
In
methanol;
at 20 - 78 ℃;
Heating / reflux;
3-chloroprop-1-ene;
at 78 - 83 ℃;
for 2h;
|
4668-00-2 Upstream products
-
67-56-1
methanol
-
681-84-5
tetramethylorthosilicate
-
98-13-5
Phenyltrichlorosilane
-
2487-90-3
trimethoxysilane
4668-00-2 Downstream products
-
58458-85-8
trimethoxy(phenylethynyl)silane
-
75-77-4
chloro-trimethyl-silane
-
122278-74-4
C4 H10 O5 Si
-
13170-06-4
(acetoxy)tri(methoxy)silane