21619-76-1 Usage
Uses
Used in the Manufacturing Industry:
3-Cyclohexenyltrimethoxysilane is used as a silane coupling agent for improving the adhesion, weatherability, and moisture resistance of materials. Its presence in formulations contributes to the enhanced performance and durability of products like silicone rubbers, adhesives, and coatings.
Used in the Production of Silicone Rubbers:
3-Cyclohexenyltrimethoxysilane is used as a reactive component to enhance the bonding and compatibility of silicone rubbers with various substrates, thereby improving their overall performance and reliability in applications that demand high durability and resistance to environmental factors.
Used in the Formulation of Adhesives:
As a silane coupling agent, 3-Cyclohexenyltrimethoxysilane is used in the development of adhesives to promote stronger bonds between different materials. Its ability to improve adhesion ensures that the adhesives are more effective in joining components in various industrial applications.
Used in the Production of Coatings:
3-Cyclohexenyltrimethoxysilane is utilized in the creation of coatings to increase their resistance to weathering and moisture. This results in coatings that offer better protection for the surfaces they are applied to, extending their service life and maintaining their appearance over time.
Check Digit Verification of cas no
The CAS Registry Mumber 21619-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,6,1 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21619-76:
(7*2)+(6*1)+(5*6)+(4*1)+(3*9)+(2*7)+(1*6)=101
101 % 10 = 1
So 21619-76-1 is a valid CAS Registry Number.
21619-76-1Relevant academic research and scientific papers
García-Domínguez, Andrés,Mondal, Rahul,Nevado, Cristina
, p. 12286 - 12290 (2019)
The potential of merging photoredox and nickel catalysis to perform multicomponent alkene difunctionalizations under visible-light irradiation is demonstrated here. Secondary and tertiary alkyl groups, as well as sulfonyl moieties can be added to the terminal position of the double bond with simultaneous arylation of the internal carbon atom in a single step under mild reaction conditions. The process, devoid of stoichiometric additives, benefits from the use of bench-stable and easy-to-handle reagents, is operationally simple, and tolerates a wide variety of functional groups.
