97802-57-8 Usage
General Description
2-(3,4-epoxycyclohexyl) ethylmethyl dimethoxysilane is a chemical compound used in the production of adhesives, sealants, and coatings. It is a colorless liquid with a molecular formula of C10H22O4Si and a molecular weight of 242.37 g/mol. The compound contains a cyclohexyl epoxide group and a silane group, making it suitable for use as a coupling agent and crosslinking agent in formulation of polymers and composites. It is also utilized as a surface treatment agent for improving the adhesion of organic coatings on inorganic substrates. Additionally, the compound has potential application in the fields of electronics, construction, and automotive industries for its ability to enhance material strength and durability. However, its use requires careful handling and storage due to its flammability and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 97802-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,0 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97802-57:
(7*9)+(6*7)+(5*8)+(4*0)+(3*2)+(2*5)+(1*7)=168
168 % 10 = 8
So 97802-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O3Si/c1-12-15(3,13-2)7-6-9-4-5-10-11(8-9)14-10/h9-11H,4-8H2,1-3H3
97802-57-8Relevant articles and documents
Unexpected silicon group transfer in difunctional alkoxy silanes
Filipkowski, Michelle A.,Petty, Herbert E.,Westmeyer, Mark D.,Schilling Jr., Curtis L.
, p. 15 - 19 (2013/09/06)
During the hydrosilylation reaction of a difunctional silane with allyl glycidyl ether (AGE), two scrambled hydrosilylation products were produced in significant amounts. This scrambling is reaction condition dependent and has been observed in a few other examples. It appears to be the first such alkoxysilane transformation to occur under these conditions, although similar siloxane transformations have been documented. This also introduces a method of preparing certain organofunctional alkyldialkoxysilanes in high purities via hydrosilylation, where the close boiling rearrangement by-products are minimized.
