80252-60-4 Usage
General Description
Vinylphenylmethylmethoxysilane is a clear, colorless liquid primarily used as a coupling agent in the production of organic-inorganic composite materials, such as resins, rubbers, and plastics. It contains a vinyl group and a methoxy group, making it a versatile chemical in various polymerization and crosslinking reactions. Vinylphenylmethylmethoxysilane can also be utilized as an adhesion promoter, improving the bonding strength between organic polymers and inorganic fillers or surfaces. Its excellent adhesion, weatherability, and resistance to moisture make it a valuable component in the formulation of coatings, adhesives, and sealants for industrial and construction applications. Additionally, it is used in the semiconductor industry as a component in the production of silicone-based materials for electrical encapsulation and protective coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 80252-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,5 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80252-60:
(7*8)+(6*0)+(5*2)+(4*5)+(3*2)+(2*6)+(1*0)=104
104 % 10 = 4
So 80252-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14OSi/c1-4-12(3,11-2)10-8-6-5-7-9-10/h4-9H,1H2,2-3H3
80252-60-4Relevant articles and documents
Diphenylchlorosilanes preparation containing phenyl vinyl organic silicon sealed end medicinal preparation method
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Paragraph 0025; 0026, (2018/11/03)
The invention discloses a method for preparing an organic silicon end-capping reagent containing phenyl vinyl by using a grignard method. The method is characterized by comprising the following steps: (1) reacting chlorobenzene or bromobenzene with magnes
Silanediyl to Sila-alkene Conversions. Generation and Rearrangement of Cyclopropylsilanediyl
Ando, Wataru,Hamada, Yoshitaka,Sekiguchi, Akira
, p. 787 - 788 (2007/10/02)
Intramolecular rearrangement of cyclopropylphenylsilanediyl to 1-phenyl-1-silacyclobutene and its ring opening to 2-phenyl-2-silabutadiene are reported.
