5290-29-9 Usage
General Description
Triethylacetoxyacetoxy silane is a chemical compound that is commonly used as a crosslinking agent in the production of silicone rubber and other silicone-based products. It is a colorless, clear liquid with a mild, fruity odor and is highly flammable. Triethylacetoxyacetoxy silane reacts with moisture to form a silicone polymer, making it a valuable component in the manufacturing of adhesives, sealants, and coatings. Its unique reactivity and ability to improve the physical properties of silicone materials make it an important ingredient in a wide range of industrial and commercial applications. However, it is important to handle and store triethylacetoxyacetoxy silane with caution due to its flammability and reactivity with water.
Check Digit Verification of cas no
The CAS Registry Mumber 5290-29-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5290-29:
(6*5)+(5*2)+(4*9)+(3*0)+(2*2)+(1*9)=89
89 % 10 = 9
So 5290-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C22H20ClN5O2/c1-25-19-18(20(29)28(22(25)30)14-15-8-5-6-11-17(15)23)27-13-7-12-26(21(27)24-19)16-9-3-2-4-10-16/h2-6,8-11H,7,12-14H2,1H3
5290-29-9Relevant articles and documents
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Bradley,Thomas
, p. 3404,3405, 3409 (1959)
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Use of Silylated Formiates as Hydrosilane Equivalents
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Paragraph 0514, (2021/09/26)
The present invention relates to a method for preparing organic compounds of formula (I) by reaction between a silylated formiate of formula (II) and an organic compound in the presence of a catalyst and optionally of an additive. The invention also relates to use of the method for preparing organic compounds of formula (I) for the preparation of reagents for fine chemistry and for heavy chemistry, as well as in the production of vitamins, pharmaceutical products, adhesives, acrylic fibres, synthetic leathers, and pesticides.
Silylation of O-H bonds by catalytic dehydrogenative and decarboxylative coupling of alcohols with silyl formates
Chauvier, Clément,Godou, Timothé,Cantat, Thibault
, p. 11697 - 11700 (2017/11/03)
The silylation of O-H bonds is a useful methodology in organic synthesis and materials science. While this transformation is commonly achieved by reacting alcohols with reactive chlorosilanes or hydrosilanes, we show herein for the first time that silylformates HCO2SiR3 are efficient silylating agents for alcohols, in the presence of a ruthenium molecular catalyst.
