76301-00-3 Usage
Uses
Used in Construction Industry:
2-(CARBOMETHOXY)ETHYLTRIMETHOXYSILANE is used as an adhesion promoter and coupling agent to enhance the bonding strength between different materials, such as concrete and metal, thereby improving the structural integrity and durability of construction materials.
Used in Automotive Industry:
In the automotive sector, 2-(CARBOMETHOXY)ETHYLTRIMETHOXYSILANE is utilized as a component in the formulation of adhesives and sealants. It ensures robust adhesion between various parts and materials, contributing to the longevity and performance of vehicles.
Used in Electronics Industry:
2-(CARBOMETHOXY)ETHYLTRIMETHOXYSILANE is employed in the electronics industry as a coupling agent in the production of silicone rubber and other materials. It helps in creating seals and coatings that are resistant to water and other environmental factors, safeguarding electronic components from damage.
Used in Advanced Material Production:
2-(CARBOMETHOXY)ETHYLTRIMETHOXYSILANE is used as a key component in the synthesis of advanced materials, such as silicone rubber, where it plays a crucial role in improving the material's adhesion to various substrates and enhancing its overall performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 76301-00-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,0 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76301-00:
(7*7)+(6*6)+(5*3)+(4*0)+(3*1)+(2*0)+(1*0)=103
103 % 10 = 3
So 76301-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O5Si/c1-9-7(8)5-6-13(10-2,11-3)12-4/h5-6H2,1-4H3
76301-00-3Relevant academic research and scientific papers
The Highly Regioselective Carbonylation of Vinylsilanes
Takeuchi, Ryo,Ishii, Naomi,Sugiura, Masaharu,Sato, Nobuhiro
, p. 4189 - 4194 (2007/10/02)
The hydroesterification of vinylsilanes, catalyzed by transition-metal complexes, afforded both β-silyl esters 2 and α-silyl esters 3 in high yield.The Pd(II) complex-catalyzed reaction showed high β-regioselectivity, whereas the Co2(CO)8-catalyzed reaction showed high α-regioselectivity.Vinylsilanes which bore trialkyl-, diphenylmethyl-, dimethylethoxy-, trimethoxy-, diphenylfluoro-, and difluorophenylsilyl groups were regioselectively, and in some cases regiospecifically, hydroesterified.Pd(II) complexes were also shown to be effective catalysts of the hydrocarboxylation of vinylsilanes.Hydrocarboxylation was β-regiospecific and gave excellent yields of β-silyl carboxylic acids.Reasonable mechanisms for the reactions are described.
