32752-37-7

Basic information

• Product Name: 1,3,5-Triazine, hexahydro-1,3,5-tris(4-methoxyphenyl)-
• CAS NO: 32752-37-7
• Molecular Formula: C24H27N3O3
• Molecular Weight: 405.497
• Mol File: 32752-37-7.mol
• Article Data: 33

Chemical Properties

• Melting Point: 126-127 °C
• Boiling Point: 605.1±55.0 °C(Predicted)
• Density: 1.178±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,3,5-Triazine, hexahydro-1,3,5-tris(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Triazine, hexahydro-1,3,5-tris(4-methoxyphenyl)-(32752-37-7)
• EPA Substance Registry System: 1,3,5-Triazine, hexahydro-1,3,5-tris(4-methoxyphenyl)-(32752-37-7)

Safety Data

• Hazardous Substances Data: 32752-37-7(Hazardous Substances Data)

Usage

Chemical structure

Hexahydro-1,3,5-triazine with three 4-methoxyphenyl groups attached

Type of compound

Triazine derivative

Common uses

Synthesis of organic compounds, pharmaceuticals, building block in polymers and dyes

Potential applications

Medicine, agriculture, materials science

Industrial processes

Versatile ingredient in various processes and products due to its unique chemical structure and properties

Upstream product

• 1353053-97-0 triethylsiloxymethyl-N,N-dimethylamine 
• 104-94-9 4-methoxy-aniline 
• 50-00-0 formaldehyd 
• 229323-97-1 2,2-dihydroperoxyadamantane 
• 51-46-7 1,3,6,8-tetraazatricyclo[4.4.1.1^3,8]dodecane 
• 115163-00-3 2-anisidine 
• 78666-54-3 N,N'-bis-(4-methoxy-phenyl)-methanediamine 

Downstream Products

• 1026620-05-2 2-{tert-butoxy-[(4-methoxy-phenylamino)-methyl]-phosphinoylmethyl}-pentanedioic acid di-tert-butyl ester 
• 914389-32-5 (+/-)-5-benzyloxycarbonyl-2-(4-methoxyphenyl)-2,5-diazaspiro[3,4]octan-1-one 
• 933782-80-0 1-(4-methoxy-phenyl)-aziridine-2-carboxylic acid methyl ester 

Relevant articles and documents

Ultrasound-assisted synthesis of substituted triazines and their corrosion inhibition behavior on N80 steel/acid interface

The three substituted triazines were synthesized by ultrasound irradiation method and characterized by FTIR, 13C NMR, and 1H NMR. The corrosion inhibition behavior of the synthesized inhibitors on N80 steel in 15% HCl was studied using electrochemical analyses and weight loss methods. All three inhibitors exhibited excellent corrosion inhibition performance, and the best inhibition effect was shown by TZ-3 (93.2% at 800 mg/L). EIS measurements suggest that the corrosion inhibition process is a charge transfer controlled. The PDP results indicated that all the triazines are mixed-type inhibitors. Langmuir adsorption model is the best fit among the other tested isotherms. These molecules can act as promising acidizing corrosion inhibitors for the oil gas industry. FTIR, AFM, and UV-vis studies corroborate the adsorption of inhibitor molecules over the metal surface.

Role of the nucleophilicity of the amino group of benzidines in the synthesis of hemiaminal ethers

This paper presents a study of the reaction between some aromatic amines and formaldehyde in ethanol. Anisidines reacting with formaldehyde produced cyclic or linear aminals (hexahydrotriazines or methanediamines) whilst benzidines produced hemiaminal eth

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.