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1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE

  • CAS:2547-66-2
  • purity:99%
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Bulk supply high purity 1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE 2547-66-2, Paid sample available

  • Molecular Formula: C24H27 N3
  • Molecular Weight: 357.498
  • Vapor Pressure: 7.94E-09mmHg at 25°C 
  • Melting Point: 49-51 °C(lit.)
     
  • Refractive Index: 1.6270 (estimate) 
  • Boiling Point: 100 °C0.005 mm Hg(lit.)
     
  • PKA: 5.46±0.20(Predicted) 
  • Flash Point: 234.5°C 
  • PSA: 9.72000 
  • Density: 1.136g/cm3 
  • LogP: 4.19280 

1,3,5-TRIBENZYLHEXAHYDRO-1,3,5-TRIAZINE(Cas 2547-66-2) Usage

Synthesis

To a round-bottomed flask (125 mL) equipped with a reflux condenser was added theappropriate amine (0.05 mmol), toluene (40 mL) and formaldehyde (37%, 4.1 mL).The solution was brought to reflux using an external oil bath and kept stirring for 30min. Then, the toluene was evaporated under reduced pressure, and the residue wasdissolved in ethyl acetate and washed with a saturated aqueous solution of sodiumchloride. After evaporation of the solvent under reduced pressure in a rotaryevaporator, the residue was purified by silica gel column chromatography usinghexane/ethyl acetate 9:1 as the eluent.

Application

1,3,5-Tribenzylhexahydro-1,3,5-triazine was used:in the synthesis of alkyl β-aminocarboxylates via trifluoromethanesulfonic acid catalyzed reaction with ketene silyl acetals;as ligand to study the assembling process of a heterogeneous Cr-based single-site ethylene trimerization catalyst by X-ray absorption spectroscopy;as ligand during conversion of Phillips Cr/SiO2 polymerisation catalyst to ethylene trimerisation catalyst after assembling new active sites on the silica surface.

InChI:InChI=1/C24H27N3/c1-4-10-22(11-5-1)16-25-19-26(17-23-12-6-2-7-13-23)21-27(20-25)18-24-14-8-3-9-15-24/h1-15H,16-21H2/p+3

2547-66-2 Relevant articles

-

Hunt,Wagner

, p. 1792,1798 (1951)

-

Structural and Thermodynamics Studies on Polyaminophosphonate Ligands for Uranyl Decorporation

Ye, Gaoyang,Roques, Jérome,Solari, Pier-Lorenzo,Den Auwer, Christophe,Jeanson, Aurélie,Brandel, Jérémy,Charbonnière, Lo?c J.,Wu, Wangsuo,Simoni, éric

, p. 2149 - 2159 (2021)

The development of actinide decorporatio...

-

McDonagh,A.F.,Smith,H.E.

, p. 8 - 12 (1968)

-

Synthesis of highly functional imidazole derivatives via assembly of 2-unsubstituted imidazole N-oxides with CH-acids and arylglyoxals

Perevalov, Valery P.,Mityanov, Vitaly S.,Lichitsky, Boris V.,Komogortsev, Andrey N.,Kuz'mina, Ludmila G.,Koldaeva, Tatyana Yu.,Miroshnikov, Vladimir S.,Kutasevich, Anton V.

, (2020)

A novel and convenient method for the sy...

Synthesis and Cytotoxic Activity of Hexahydro-1,3,5-triazine Derivatives through Ring Condensation

Bae, Song Mi,Kang, Sung Young,Song, Ju Hyun

, p. 840 - 846 (2021)

As a part of a research program for phar...

Synthesis of α-Amino Tertiary Alkylperoxides by Lewis Acid-Catalyzed Peroxidation of 1,3,5-Triazines

Liu, Lijuan,Shi, Zhichao,Zhang, Xun,Zhan, Feng,Lin, Jin-Shun,Jiang, Yuyang

supporting information, p. 3487 - 3491 (2021/09/20)

α-Substituted peroxides have been found ...

2547-66-2 Process route

benzylamine
100-46-9

benzylamine

(+/-)-2-(1,3,5-dithiazinan-5-yl)-1-methylethanol
633336-01-3

(+/-)-2-(1,3,5-dithiazinan-5-yl)-1-methylethanol

1,3,5-Tribenzyl-1,3,5-triazacyclohexane
2547-66-2

1,3,5-Tribenzyl-1,3,5-triazacyclohexane

3-amino-2-propanol
78-96-6,1674-56-2

3-amino-2-propanol

Conditions
Conditions Yield
In tetrahydrofuran; at 20 ℃;
95%
benzylamine
100-46-9

benzylamine

5-(2-hydroxyethyl)hexahydro-1,3,5-dithiazine
88891-55-8

5-(2-hydroxyethyl)hexahydro-1,3,5-dithiazine

1,3,5-Tribenzyl-1,3,5-triazacyclohexane
2547-66-2

1,3,5-Tribenzyl-1,3,5-triazacyclohexane

ethanolamine
141-43-5

ethanolamine

Conditions
Conditions Yield
at 20 ℃; for 24h;
95%

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