19338-12-6

Basic information

• Product Name: 2 4-DIAMINO-6-(4-METHYLPHENYL)-1 3 5-
• Synonyms: 2 4-DIAMINO-6-(4-METHYLPHENYL)-1 3 5-;1,3,5-Triazine-2,4-diaMine, 6-(4-Methylphenyl)-;2,4-Diamino-6-(4-methylphenyl)-1,3,5-triazine, 4-(4,6-Diamino-1,3,5-triazin-2-yl)toluene;6-(4-Methylphenyl)-1,3,5-triazine-2,4-diamine
• CAS NO: 19338-12-6
• Molecular Formula: C₁₀H₁₁N₅
• Molecular Weight: 201.232
• Product Categories: Heterocyclic Compounds;Building Blocks;Heterocyclic Building Blocks;Triazines
• Mol File: 19338-12-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 239.5-243.5 °C(lit.)
• Boiling Point: 490.6 °C at 760 mmHg
• Flash Point: 282.5 °C
• Appearance: /
• Density: 1.296 g/cm³
• Vapor Pressure: 9.01E-10mmHg at 25°C
• Refractive Index: 1.676
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2 4-DIAMINO-6-(4-METHYLPHENYL)-1 3 5-(CAS DataBase Reference)
• NIST Chemistry Reference: 2 4-DIAMINO-6-(4-METHYLPHENYL)-1 3 5-(19338-12-6)
• EPA Substance Registry System: 2 4-DIAMINO-6-(4-METHYLPHENYL)-1 3 5-(19338-12-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37
• WGK Germany: 3
• Hazardous Substances Data: 19338-12-6(Hazardous Substances Data)

Usage

General Description

2,4-Diamino-6-(4-Methylphenyl)-1,3,5- is a chemical compound with specific functional groups, such as amine and methyl groups. Its structural composition suggests that it may be aromatic due to the presence of a phenyl group. The molecule could possibly be involved in a range of applications, including the synthesis of other complex molecules in industrial or laboratory settings. However, no specific information on its actual use or safety is readily available, which implies it may be a less common or specific-use compound. It is essential to handle it using appropriate personal protective equipment and in accordance with local legal guidelines and standards due to its chemical nature.

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

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

Downstream Products

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

Relevant articles and documents

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

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.

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.