19338-12-6

Usage

Uses

Used in Chemical Synthesis:
2,4-Diamino-6-(4-Methylphenyl)-1,3,5is used as a chemical intermediate for the synthesis of other complex molecules in various industries. Its functional groups, such as amine and methyl, make it a versatile building block for creating a wide range of compounds.
Used in Research and Development:
In the field of research and development, 2,4-Diamino-6-(4-Methylphenyl)-1,3,5is used as a starting material for exploring new chemical reactions and pathways. Its unique structure allows scientists to investigate its potential applications in various areas, such as pharmaceuticals, materials science, or catalysis.
Used in Pharmaceutical Industry:
2,4-Diamino-6-(4-Methylphenyl)-1,3,5is used as a key component in the development of new pharmaceutical compounds. Its structural features may contribute to the design of novel drugs with specific therapeutic properties, such as improved efficacy or reduced side effects.
Used in Material Science:
In material science, 2,4-Diamino-6-(4-Methylphenyl)-1,3,5is used as a component in the creation of new materials with unique properties. Its incorporation into polymers or other materials may lead to the development of advanced materials with applications in various industries, such as electronics, automotive, or aerospace.

InChI:InChI=1/C10H11N5/c1-6-2-4-7(5-3-6)8-13-9(11)15-10(12)14-8/h2-5H,1H3,(H4,11,12,13,14,15)

Upstream product

• 3397-62-4 2-Chloro-4,6-diamino-1,3,5-triazine 
• 5720-05-8 4-methylphenylboronic acid 
• 104-85-8 para-methylbenzonitrile 
• 127099-85-8 N-Cyanoguanidine 

Downstream Products

• 186834-90-2 N-(4-Isobutyrylamino-6-p-tolyl-[1,3,5]triazin-2-yl)-isobutyramide 
• 1061683-98-4 [Ag(2,4-diamino-p-tolyl-1,3,5-triazine)(PF₆)]n 

Relevant academic research and scientific papers

Carbon and Nitrogen Based Nanosheets as Fluorescent Probes with Tunable Emission

2D carbon and nitrogen based semiconductors (CN) have attracted widespread attention for their possible use as low-cost and environmentally friendly materials for various applications. However, their limited solution-dispersibility and the difficulty in p

2,4,6-trisubstituted-1,3,5-s-triazine compound and preparation and application thereof

The invention provides a 2,4,6-trisubstituted-1,3,5-s-triazine compound as well as preparation and application thereof, and biguanide or dimethyl biguanide hydrochloride is used as an initial raw material to react with a cyano compound under an alkaline condition to prepare the 2,4,6-trisubstituted-1,3,5-s-triazine compound. The invention provides a simple and convenient synthetic method of a 2,4,6-trisubstituted-1,3,5-s-triazine compound, and the compound provided by the invention can be applied to preparation of an anti-myelogenous leukemia medicine, namely an enasidenib medicine. Compared with the prior art, the method for preparing the enasidenib has the advantages that two-step reaction is reduced, the use of a halogenating reagent is avoided, and the method is a green and environment-friendly chemical process. The structural formula I is shown in the specification.

Microwave-assisted clean synthesis of 6-aryl-2,4-diamino-1,3,5-triazines in [bmim][PF6]

An efficient and green approach was developed to prepare 6-aryl-2,4-diamino-1,3,5-triazines from corresponding arylnitriles and dicyanodiamide in ionic liquid [bmim][PF6] under computer-controlled microwave irradiation. Particularly valuable features of this method included the short reaction time, good yield, convenient operation and eco-friendly solvent.

Synthesis of 6-aryl-2,4-diamino-pyrimidines and triazines using palladium catalysed Suzuki cross-coupling reactions

The high yielding synthesis of 6-aryl-2,4-diaminopyrimidines and triazines via palladium catalysed Suzuki cross-coupling reactions of commercially available 6-chloro-2,4-diaminopyrimidine 1 or 6-chloro-2,4-diaminotriazine 8 and aryl boronic acids are desc

Model Systems for Flavoenzyme Activity. Regulation of Flavin Recognition via Modulation of Receptor Hydrogen-Bond Donor-Acceptor Properties

We have synthesized a new family of receptors for flavins based on 6-aryl-2,4-(acyldiamino)-s-triazines. In these synthetic hosts, systematic variation of the spatially remote substituents on the 6-aryl ring alters the hydrogen-bond-donating abilities of the amide functionality and the hydrogen-bond-accepting properties of the triazine N(3). This variation results in a strong modulation of the efficiency of flavin binding, with association constants for the receptor flavin complexes ranging over an 8-fold range.