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2-chloro-4,6-diphenyl-1,3,5-triazine

Basic information Uses Safety Supplier Related

2-chloro-4,6-diphenyl-1,3,5-triazine Basic information

Product Name:
2-chloro-4,6-diphenyl-1,3,5-triazine
Synonyms:
  • 2-chloro-4,6-diphenyl-1,3,5-triazine
  • 2-chloro-4,6-dipheyl-1,3,5-triazine
  • 1,3,5-Triazine, 2-chloro-4,6-diphenyl-
  • ClTPTA
  • 2-Chloro-4,6-diphenyl-1,3,5-triazine >
  • 2-chloro-4,6-diphenyl-1,3,5-triazine ISO 9001:2015 REACH
  • PTZ-Cl
  • CITPTA
CAS:
3842-55-5
MF:
C15H10ClN3
MW:
267.71
Product Categories:
  • OLED
  • 1,3,5-triazine
Mol File:
3842-55-5.mol
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2-chloro-4,6-diphenyl-1,3,5-triazine Chemical Properties

Melting point:
138-140℃
Boiling point:
485.1±28.0 °C(Predicted)
Density 
1.265±0.06 g/cm3(Predicted)
refractive index 
1.57
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Soluble in toluene.
form 
powder to crystal
pka
-0.19±0.10(Predicted)
color 
White to Yellow to Orange
InChI
InChI=1S/C15H10ClN3/c16-15-18-13(11-7-3-1-4-8-11)17-14(19-15)12-9-5-2-6-10-12/h1-10H
InChIKey
DDGPPAMADXTGTN-UHFFFAOYSA-N
SMILES
N1=C(C2=CC=CC=C2)N=C(C2=CC=CC=C2)N=C1Cl
CAS DataBase Reference
3842-55-5
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Safety Information

HS Code 
2933698090
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2-chloro-4,6-diphenyl-1,3,5-triazine Usage And Synthesis

Uses

2-chloro-4,6-diphenyl-1,3,5-triazine is a useful research chemical.

Description

2-Chloro-4, 6-Diphenyl-1, 3, 5-Triazine is an OLED intermediate. It appears white powder at room temperature (20°C).

Chemical Properties

yellow powder

Uses

A rational synthesis of kyaphenine (2:4:6-triphenyl-1:3:5-triazine) has been effected by reaction of 2-chloro-4:6-diphenyl-1:3:5-triazine with phenylmagnesium bromide.

Uses

2-chloro-4,6-diphenyl-1,3,5-triazine is an organic compound. Its main uses are:
1 It is used to prepare benzimidazole compounds and derivatives and organic electron transport materials. Organic light emitting diodes (OLEDs) have important applications in new electroluminescent displays and lighting.
2. It is used to prepare organic small molecule electron transport materials.

Synthesis Reference(s)

The Journal of Organic Chemistry, 34, p. 4125, 1969 DOI: 10.1021/jo01264a079
Synthesis, p. 841, 1980 DOI: 10.1055/s-1980-29230

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