6639-47-0

Basic information

• Product Name: 1,3,5-Triazine, hexahydro-1,3, 5-tris (4-methylphenyl)-
• Synonyms: 1,3,5-Triazine, hexahydro-1,3, 5-tris (4-methylphenyl)-;1,3,5-Tris(4-methylphenyl)hexahydro-1,3,5-triazine;Hexahydro-1,3,5-tris(4-methylphenyl)-1,3,5-triazine
• CAS NO: 6639-47-0
• Molecular Formula: C₂₄H₂₇N₃
• Molecular Weight: 357.49
• Mol File: 6639-47-0.mol
• Article Data: 19

Chemical Properties

• Boiling Point: 557.5°C at 760 mmHg
• Flash Point: 317°C
• Appearance: /
• Density: 1.113g/cm³
• Vapor Pressure: 1.82E-12mmHg at 25°C
• Refractive Index: 1.617
• CAS DataBase Reference: 1,3,5-Triazine, hexahydro-1,3, 5-tris (4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Triazine, hexahydro-1,3, 5-tris (4-methylphenyl)-(6639-47-0)
• EPA Substance Registry System: 1,3,5-Triazine, hexahydro-1,3, 5-tris (4-methylphenyl)-(6639-47-0)

Safety Data

• Hazardous Substances Data: 6639-47-0(Hazardous Substances Data)

Usage

Chemical structure

A triazine ring with three 4-methylphenyl groups attached.

Physical state

Colorless to pale yellow solid.

Solubility

Insoluble in water, soluble in organic solvents.

Applications

a. Production of specialty chemicals.
b. Intermediate in the synthesis of pharmaceuticals and agrochemicals.
c. Building block in the synthesis of various polymers and materials.

Thermal stability

High thermal stability, making it suitable for various industrial applications.

InChI:InChI=1/C24H27N3/c1-19-4-10-22(11-5-19)25-16-26(23-12-6-20(2)7-13-23)18-27(17-25)24-14-8-21(3)9-15-24/h4-15H,16-18H2,1-3H3

Upstream product

• 50-00-0 formaldehyd 
• 106-49-0 p-toluidine 
• 88919-94-2 4-toluidine 
• 51-46-7 1,3,6,8-tetraazatricyclo[4.4.1.1^3,8]dodecane 
• 1353053-97-0 triethylsiloxymethyl-N,N-dimethylamine 
• 229323-97-1 2,2-dihydroperoxyadamantane 
• 88876-21-5 N-allyl-N-ethyl-p-toluidine 
• 17450-22-5 bis(4-methylphenylamino)methane 
• 98-01-1 furfural 
• 3533-10-6 3-(2-chlorophenyl)-2-cyanoprop-2-enamide 

Downstream Products

• 5546-18-9 N-p-tolyl-glycine amide 
• 73086-50-7 2-amino-5-methyl-N-tolylbenzylamine 
• 3299-61-4 N,N'-Di-p-tolyloxalamide 
• 109423-14-5 Trifluoro-acetic acid [p-tolyl-(2,2,2-trifluoro-acetyl)-amino]-methyl ester 
• 32328-79-3 4-methyl-N-methyleneaniline 
• 168907-82-2 1-phenyl-3,5-di-p-tolyl-tetrahydro-[1,3,5]triazin-2-one 
• 17450-22-5 bis(4-methylphenylamino)methane 
• 495-48-7 azoxybenzene 
• 529-81-7 Troeger's base 
• 6638-23-9 1-<(4-Methylphenylamino)methyl>-2-naphthol 
• 116757-17-6 3-(Azidomethyl)-6-methyl-2(3H)-benzothiazolone 
• 116757-16-5 6-Methyl-3-(p-tolylthiomethyl)-2(3H)-benzothiazolone 

Relevant articles and documents

Divergent Synthesis of Aziridine and Imidazolidine Frameworks under Blue LED Irradiation

We develop a visible light-promoted divergent cycloaddition of α-diazo esters with hexahydro-1,3,5-triazines, leading to a series of aziridine and imidazolidine frameworks in average good yield, by simply changing the reaction media used. It is noteworthy that the reaction occurs under sole visible light irradiation without the need for exogenous photoredox catalysts. More significantly, a reasonable reaction mechanism was proposed on the basis of the control experiments and density functional theory calculation results.

3, 4-dihydro-2H-1, 3-thiazine derivative and preparation method thereof

The invention belongs to the field of chemical synthesis, and particularly relates to a 3, 4-dihydro-2H-1, 3-thiazine derivative and a preparation method thereof. The structural formula of the 3, 4-dihydro-2H-1, 3-thiazine derivative is shown in the speci

Activation Relay on Rhodium-Catalyzed C-H Aminomethylation in Cooperation with Photoredox Catalysis

A site selective C-H aminomethylation at indole's C3 position has been achieved by merging rhodium(III)-catalyzed C-H activation and photoredox catalysis in a one-pot manner. An investigation of the mechanistic insights rationalized the essence of the activation relay and the combination mode.