19302-93-3 Usage
General Description
Trityl methacrylate is a chemical compound that is commonly used in the production of polymer materials. It is a methacrylate monomer, meaning it contains a specific chemical structure that makes it capable of polymerization. Trityl methacrylate is often used as a component in adhesives, sealants, and coatings, where its polymerization properties contribute to the strength and durability of the final product. It is also used in the production of dental materials and as a component in photoresists for microelectronics. Trityl methacrylate is known for its high refractive index, making it useful in optical applications as well. Overall, trityl methacrylate is a versatile compound with a variety of industrial and commercial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19302-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,0 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19302-93:
(7*1)+(6*9)+(5*3)+(4*0)+(3*2)+(2*9)+(1*3)=103
103 % 10 = 3
So 19302-93-3 is a valid CAS Registry Number.
19302-93-3Relevant articles and documents
Stereogradient polymers formed by controlled/living radical polymerization of bulky methacrylate monomers
Ishitake, Kenji,Satoh, Kotaro,Kamigaito, Masami,Okamoto, Yoshio
, p. 1991 - 1994 (2009)
(Chemical Equation Presented) Life RAFT: A bulky methacrylate monomer, triphenylmethyl methacrylate (TrMA), was polymerized with reversible addition-fragmentation chain transfer (RAFT) agents. Stereogradient polymers in which the isospecificity increased
Process for preparing triarylmethyl methacrylate
-
, (2008/06/13)
A triarylmethyl methacrylate is produced by reacting methacrylic acid with a triarylmethylating agent in an inert, organic solvent containing therein an excess amount of an amine or in the presence of an anion exchanger.
A FACILE PROCEDURE FOR O-TRITYLATION
Murata, S.,Noyori, R.
, p. 2107 - 2108 (2007/10/02)
The title operation is achieved via readily accessible organosilicon compounds.
