76301-00-3 Usage
General Description
2-(carbomethoxy)ethyltrimethoxysilane is a chemical compound used as a coupling agent and adhesion promoter in various applications, including in the production of advanced materials such as silicone rubber, adhesives, coatings, and sealants. It is a silane compound with a trimethoxysilane group, which allows it to react with surfaces and polymers containing hydroxyl groups, enhancing their adhesion and water resistance. The presence of the carbomethoxy and ethyl groups in the molecule contributes to its reactivity and versatility in bonding with a wide range of substrates. This chemical is commonly used in industries such as construction, automotive, and electronics to improve the performance and durability of materials and products.
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 articles and documents
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.
