5833-57-8 Usage
Uses
Used in Sealant Industry:
Acetoxymethyldimethylacetoxysilane is used as a crosslinking agent for improving the bonding and adhesion properties of sealants. Its reactivity and functional groups enable it to create strong and durable bonds, ensuring the sealants' performance and reliability in various applications.
Used in Adhesive Industry:
In the adhesive industry, Acetoxymethyldimethylacetoxysilane is utilized as a crosslinking agent to enhance the bonding strength and durability of adhesives. Its ability to bind effectively to different surfaces contributes to the improved performance of adhesives in various bonding applications.
Used in Coating Industry:
Acetoxymethyldimethylacetoxysilane is employed as a crosslinking agent in the formulation of coatings. Its unique chemical structure and reactivity contribute to the development of coatings with enhanced bonding, adhesion, and durability properties, making them suitable for various substrates and applications.
Used in Polymer Industry:
In the polymer industry, Acetoxymethyldimethylacetoxysilane is used as a crosslinking agent to improve the properties of various polymers. Its ability to effectively bind to a range of surfaces and substrates allows for the creation of polymers with enhanced bonding, adhesion, and overall performance.
Check Digit Verification of cas no
The CAS Registry Mumber 5833-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5833-57:
(6*5)+(5*8)+(4*3)+(3*3)+(2*5)+(1*7)=108
108 % 10 = 8
So 5833-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H14O4Si/c1-6(8)10-5-12(3,4)11-7(2)9/h5H2,1-4H3
5833-57-8Relevant academic research and scientific papers
Synthesis and Properties of (Hydroxymethyl)diorganylsilanes
Tacke, Reinhold,Lange, Hartwig,Bentlage, Anke
, p. 3673 - 3677 (2007/10/02)
The synthesis of the (hydroxymethyl)diorganylsilanes R1R2Si(H)CH2OH (4a: R1 = R2 = CH3, 2-silaisobutanol; 4b: R1 = CH3, R2 = C6H5; 4c: R1 = R2 = C6H5) is achieved by the reaction of R1R2Si(Cl)CH2Cl (2a - c) with AcOH/NEt3 to R1R2Si(OAc)CH2OAc (3a - c), fo
