1493-45-4 Usage
Chemical structure
A chemical compound with a triazine ring structure and fluorine and phenyl substituents.
Family
A member of the triazine family of compounds.
Applications
Known for their diverse range of applications in various industries, including agriculture, pharmaceuticals, and materials science.
Fluoro and diphenyl groups
These groups on the triazine ring contribute to its unique chemical and physical properties.
Potential uses
Useful in the development of new materials and pharmaceuticals.
Building block
May have potential applications as a building block for the synthesis of new drugs, agrochemicals, or other advanced materials.
Research and testing
Additional research and testing are necessary to fully understand and harness the potential of 1,3,5-Triazine, 2-fluoro-4,6-diphenylin various industrial and scientific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1493-45-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1493-45:
(6*1)+(5*4)+(4*9)+(3*3)+(2*4)+(1*5)=84
84 % 10 = 4
So 1493-45-4 is a valid CAS Registry Number.
1493-45-4Relevant articles and documents
Rhodium-catalyzed synthesis of unsymmetric di(heteroaryl) compounds via heteroaryl exchange reactions
Arisawa, Mieko
, p. 643 - 648 (2019/04/30)
Unsymmetric di(heteroaryl) HetAr–X–HetAr′ compounds have flexible and rigid groups, and are expected to exhibit various biological activities by interacting with proteins and nucleic acids. Then, synthesis of such compounds is critical for the development of drugs. Unsymmetric HetAr-X-HetAr′ compounds were efficiently synthesized by rhodium-catalyzed heteroaryl exchange reactions, which involved equilibrium control by judicious design of organic heteroaryl reagents. This method allows synthesis of unsymmetric HetAr–O–HetAr′, HetAr–S–HetAr′, and HetAr–CH2–HetAr′ compounds as well as HetAr–F compounds from heteroaryl aryl ethers and heteroaryl reagents. The rhodium-catalyzed heteroaryl exchange reaction was also applied to the synthesis of C–N-linked di(heteroaryl) compounds from N-benzoyl heteroarenes and heteroaryl aryl ethers. The synthesis has a broad applicability, which gives a diversity of novel unsymmetric HetAr–X–HetAr′ and C–N-linked di(heteroaryl)s compounds containing five- and six-membered heteroarenes.
