35838-12-1 Usage
Uses
Used in Coatings and Adhesives:
(2,4,6-trioxo-1,3,5-triazine-1,3H,5H,6H)-tri-2,1-ethanediyl trimethacrylate is used as a cross-linking agent in the formulation of coatings and adhesives. Its ability to crosslink with other monomers and polymers enhances the mechanical and thermal properties of the final product, resulting in improved durability and performance.
Used in Composite Materials:
In the composite materials industry, (2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tri-2,1-ethanediyl trimethacrylate is used as a key component in the production of high-performance polymers. Its reactive nature allows it to form strong bonds with other materials, leading to enhanced structural integrity and improved overall performance of the composite.
Used in Dental Restorative Materials:
(2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tri-2,1-ethanediyl trimethacrylate is used as a monomer in the manufacturing of dental restorative materials. Its excellent mechanical and thermal properties make it an ideal choice for creating durable and long-lasting dental fillings and other restorative materials.
Used in High-Performance Polymers:
In the production of high-performance polymers, (2,4,6-trioxo-1,3,5-triazine-1,3,5(2H,4H,6H)-triyl)tri-2,1-ethanediyl trimethacrylate is used as a critical component. Its high reactivity and ability to crosslink with other monomers and polymers contribute to the development of polymers with superior mechanical and thermal properties, suitable for use in demanding applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 35838-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,3 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35838-12:
(7*3)+(6*5)+(5*8)+(4*3)+(3*8)+(2*1)+(1*2)=131
131 % 10 = 1
So 35838-12-1 is a valid CAS Registry Number.
35838-12-1Relevant academic research and scientific papers
Dubosclard-Gottardi, Christine,Caubere, Paul,Fort, Yves
, p. 2561 - 2572 (1995)
The selective formulation of ω-isocyanatoalkyl (meth)acrylates may be conveniently obtained by simple condensation of potassium cyanate with ω-halogeno-alkyl (meth)acrylates under appropriated phase transfer catalytic conditions. Depending on the reaction media and the temperature, these isocyanate derivatives may be isolated, trimerized to the corresponding isocyanurates or trapped in situ as carbamates or ureas compounds.
