63823-06-3 Usage
Description
[3-(ethenylsulfanyl)propyl](trimethoxy)silane is a silane compound characterized by the molecular formula C9H20O3SSi. It features a trimethoxy substituent and an ethenylsulfanylpropyl functional group, which contribute to its versatile applications in various industries.
Uses
Used in Chemical Synthesis:
[3-(ethenylsulfanyl)propyl](trimethoxy)silane is used as a crosslinking agent for the synthesis of silane-modified polymers, such as silicone rubbers and resins. Its presence enhances the mechanical properties and durability of these materials.
Used in Adhesion and Surface Modification:
In the field of material science, [3-(ethenylsulfanyl)propyl](trimethoxy)silane is used as a coupling agent to promote the adhesion of organic polymers to inorganic surfaces. This improves the overall performance and durability of the bonded materials.
Used in the Production of Coatings, Adhesives, and Sealants:
[3-(ethenylsulfanyl)propyl](trimethoxy)silane is also utilized in the formulation of coatings, adhesives, and sealants. Its inclusion in these products serves to improve their material properties, such as adhesion, flexibility, and resistance to environmental factors.
Used in the Manufacturing of Mineral Fillers:
As a surface modifier for mineral fillers, [3-(ethenylsulfanyl)propyl](trimethoxy)silane enhances the compatibility and dispersion of these fillers within polymer matrices, leading to improved material properties and performance.
Check Digit Verification of cas no
The CAS Registry Mumber 63823-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63823-06:
(7*6)+(6*3)+(5*8)+(4*2)+(3*3)+(2*0)+(1*6)=123
123 % 10 = 3
So 63823-06-3 is a valid CAS Registry Number.
63823-06-3Relevant articles and documents
Preparation of silicon-containing vinyl ethers and vinyl thioethers
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, (2008/06/13)
Process for preparing silicon-containing vinyl ethers and vinyl thioethers of the general formula I STR1 where the variables have the following meanings: X is oxygen or sulfur, R1 is C1 -C20 -alkylene, C3 -C12 -cycloalkylene or C6 -C10 -arylene, R2, R3 and R4 are hydrogen, C1 -C20 -alkyl, C3 -C12 -cycloalkyl, C1 -C12 -alkoxy, phenoxy, heteroaryl or together with R1 form a C3 -C12 -cycle, by reaction of silicon-containing alcohols or thiols of the general formula II STR2 where the variables have the meaning indicated above, with acetylene, by carrying out the reaction in phenyl methyl sulfoxide, dimethyl sulfoxide, sulfolane or hexamethylphosphoramide in the presence of an alkali metal hydroxide.