3842-53-3

Usage

Uses

Used in Pharmaceutical Industry:
4-chloro-6-phenyl-1,3,5-triazin-2-amine is used as a synthetic intermediate for the production of pharmaceuticals. Its unique chemical structure allows it to be a key component in the synthesis of various drugs, contributing to the development of new medications and therapies.
Used in Pesticide Industry:
In the pesticide industry, 4-chloro-6-phenyl-1,3,5-triazin-2-amine is utilized as a synthetic intermediate in the creation of pesticides. Its chemical properties make it suitable for the development of effective and targeted pest control solutions.
Used in Organic Compounds Synthesis:
4-chloro-6-phenyl-1,3,5-triazin-2-amine is used as a building block in the synthesis of various organic compounds. Its versatile structure allows it to be incorporated into a wide range of chemical reactions, leading to the production of diverse organic molecules with different applications.
Used in Functional Materials Development:
4-chloro-6-phenyl-1,3,5-triazin-2-amine is also used in the development of functional materials. Its unique properties and structure make it a valuable component in the creation of materials with specific functions, such as sensors, catalysts, or other advanced materials with specialized applications.

Upstream product

• 100-58-3 phenylmagnesium bromide 
• 1700-02-3 2,4-dichloro-6-phenyl-1,3,5-triazine 
• 933-20-0 4,6-dichloro-1,3,5-triazin-2-amine 
• 611-74-5 N,N-dimethylbenzamide 
• 127099-85-8 N-Cyanoguanidine 

Downstream Products

• 1426925-58-7 C₂₁H₁₄N₄O 
• 30369-74-5 4-amino-6-phenyl-1,3,5-triazine-2-thiol 

Relevant academic research and scientific papers

Crystal Structure and Subsequent Ligand Design of a Nonriboside Partial Agonist Bound to the Adenosine A2AReceptor

In this study, we determined the crystal structure of an engineered human adenosine A2A receptor bound to a partial agonist and compared it to structures cocrystallized with either a full agonist or an antagonist/inverse agonist. The interaction between the partial agonist, belonging to a class of dicyanopyridines, and amino acids in the ligand binding pocket inspired us to develop a small library of derivatives and assess their affinity in radioligand binding studies and potency and intrinsic activity in a functional, label-free, intact cell assay. It appeared that some of the derivatives retained the partial agonist profile, whereas other ligands turned into inverse agonists. We rationalized this remarkable behavior with additional computational docking studies.

ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL HAVING SILICON-CONTAINING FOUR MEMBERED RING STRUCTURE, AND ORGANIC ELECTROLUMINESCENT ELEMENT

Provided are a material for an organic electroluminescent element formed of a silicon-containing four-membered ring compound, and an organic electroluminescent element using the material. The material for an organic electroluminescent element is formed of

The Synthesis of Alkyl- and Aryl-Substituted 1,3,5-Triazines

The reaction of chloromethyleneiminium salts with N-cyanoamidines provides a new and versatile route to alkyl- and aryl-substituted 1,3,5-triazines.Variation of substituents in the starting materials allows the synthesis of monoaryl-, diaryl-, alkyl-aryl- and certain mono- and di-alkyl-1,3,5-triazines bearing a variety of other substituents including hydrogen, chlorine and O-, S- and N-radicals.The generally good yields, ready availability of starting materials, and the scope and facility of the reaction make it the method of choice for the synthesis of 1,3,5-triazines with these substitution patterns.