5577-70-8 Usage
Uses
Used in Chemical and Materials Science Industry:
(Methacryloxymethyl)dimethylethoxysilane is used as a coupling agent for bonding organic materials to inorganic surfaces, facilitating improved adhesion and integration between different materials.
Used in Coatings Production:
(Methacryloxymethyl)dimethylethoxysilane is used as a key component in the formulation of coatings to enhance their adhesion properties, making them more durable and resistant to water.
Used in Adhesives Production:
(Methacryloxymethyl)dimethylethoxysilane is used in the production of adhesives to improve their bonding capabilities and increase their resistance to water, ensuring stronger and longer-lasting bonds.
Used in Sealants Production:
(Methacryloxymethyl)dimethylethoxysilane is used as an essential ingredient in sealants to boost their adhesive qualities and water resistance, providing a more effective sealing solution.
Check Digit Verification of cas no
The CAS Registry Mumber 5577-70-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5577-70:
(6*5)+(5*5)+(4*7)+(3*7)+(2*7)+(1*0)=118
118 % 10 = 8
So 5577-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H17N3O8S/c20-7-9-27-8-6-17-15-5-4-14(11-16(15)19(23)24)28(25,26)13-3-1-2-12(10-13)18(21)22/h1-5,10-11,17,20H,6-9H2
5577-70-8Relevant academic research and scientific papers
The Hydrolysis/Condensation Behaviour of Methacryloyloxyalkylfunctional Alkoxysilanes: Structure-Reactivity Relations
Altmann, Stefan,Pfeiffer, Juergen
, p. 1081 - 1092 (2007/10/03)
Various methacryloyloxymethylalkoxysilanes have been synthesized by nucleophilic substitution reactions starting from chloromethylalkoxysilanes under phase transfer catalysis conditions. The compounds thus obtained show an exceptionally high degree of reactivity with regard to hydrolysis and condensation both under acidic as well as under basic conditions compared to the established 3-methacryloyloxypropyltrimethoxysilane. A mechanistic model for this high reactivity by intramolecular activation is discussed.
