5118-79-6 Usage
Uses
Used in Plastics Industry:
6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine) is used as a curing agent in epoxy resins for enhancing the durability and longevity of plastic materials.
Used in Dyes and Pigments Industry:
6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine) is used as a key component in the production of dyes and pigments, providing high thermal stability and UV resistance to the final products.
Used in Polymer Production:
6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine) is used as a crosslinking agent in the production of polymers, improving their overall stability and performance.
Due to its versatility and stability, 6,6'-(2,1-Phenylene)bis(1,3,5-triazine-2,4-diamine) is in high demand across various industrial applications, making it an essential component in the manufacturing of a wide range of products.
Check Digit Verification of cas no
The CAS Registry Mumber 5118-79-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,1 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5118-79:
(6*5)+(5*1)+(4*1)+(3*8)+(2*7)+(1*9)=86
86 % 10 = 6
So 5118-79-6 is a valid CAS Registry Number.
5118-79-6Relevant academic research and scientific papers
Green synthesis and self-association of 2,4-diamino-1,3,5-triazine derivatives
Diaz-Ortiz, Angel,Elguero, Jose,Foces-Foces, Concepcion,De La Hoz, Antonio,Moreno, Andres,Del Carmen Mateo, Maria,Sanchez-Migallon, Ana,Valiente, Gema
, p. 952 - 958 (2007/10/03)
2,4-Diamino-1,3,5-triazines have been prepared by reaction of dicyandiamide with nitriles under microwave irradiation, a method that can be considered as a green procedure due to the reduction in the use of solvents during synthesis and purification, the short reaction time and the simplicity of the procedure. The structures have been confirmed in solution by NMR spectroscopy. Variable temperature experiments have been used to calculate the free energy of activation for rotation about the amino-triazine bond. The crystal structures of three 2,4-diamino-6-R-1,3,5-triazine derivatives (3a: R = phenyl, 3i: R = 1-piperidino and 3g: R = 1-phenylpyrazol-3-yl) have been determined by X-ray analysis. The N-H...N interactions change from structure to structure, resulting in a variation from pseudo-honeycomb networks to corrugated rosette layers.
