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