17980-64-2 Usage
Uses
Used in Adhesives and Coatings Industry:
METHYLTRIS(2-METHOXYETHOXY)SILANE is used as a coupling agent and adhesion promoter for improving the bonding strength and durability of adhesives, coatings, and sealants. It helps in creating strong and long-lasting bonds between different materials.
Used in Manufacturing of Silane-Modified Polymers:
METHYLTRIS(2-METHOXYETHOXY)SILANE is utilized in the production of silane-modified polymers, which exhibit enhanced properties such as improved mechanical strength, thermal stability, and chemical resistance. These polymers find applications in various industries, including automotive, aerospace, and electronics.
Used as a Surface Treatment Agent for Glass and Metal Substrates:
METHYLTRIS(2-METHOXYETHOXY)SILANE is employed as a surface treatment agent for glass and metal substrates, providing a water repellent and durable coating. This treatment enhances the performance and longevity of these materials in various applications, such as architectural glass, automotive windows, and metal components.
Check Digit Verification of cas no
The CAS Registry Mumber 17980-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,8 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17980-64:
(7*1)+(6*7)+(5*9)+(4*8)+(3*0)+(2*6)+(1*4)=142
142 % 10 = 2
So 17980-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H24O6Si/c1-11-5-8-14-17(4,15-9-6-12-2)16-10-7-13-3/h5-10H2,1-4H3
17980-64-2Relevant academic research and scientific papers
SYMMETRICAL AND UNSYMMETRICAL ORGANOSILICON MOLECULES AND ELECTROLYTE COMPOSITIONS
-
Page/Page column 37, (2014/03/26)
Described are organosilicon electrolyte compositions having improved thermostability and electrochemical properties and electrochemical devices that contain the organosilicon electrolyte compositions.
Chiral Acylsilanes in Organic Synthesis. Diastereoselective 1,2 Additions to Racemic Alkoxymethyl-Substituted Acylsilanes
Bienz, Stefan,Chapeaurouge, Alexander
, p. 1477 - 1488 (2007/10/02)
The synthesis of the three alkoxymethyl-sustituted acylsilanes 1-3 is described (Schemes 1 and 2).Their reactions with NaBH4 as well as PhLi gave the corresponding alcohols with moderate to good diastereoisomeric induction (up to 78percent de; see Table), depending upon the solvent used (Scheme 3).The results indicate that in Et2O, the reactions with PhLi proceed via 6-membered chelates (see C in Scheme 4) leading to the products with high de's (74 - 78percent).In THF, these chelates are not formed, and as a consequence, the additions take place with reversed and lower stereoselectivities (34 - 50percent de).
