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2,4-Dichloro-6-phenyl-1,3,5-triazine

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2,4-Dichloro-6-phenyl-1,3,5-triazine Basic information

Product Name:
2,4-Dichloro-6-phenyl-1,3,5-triazine
Synonyms:
  • 2,4-Dichloro-6-phenyl-1,3,5-triazine 98%
  • 4,6-DICHLORO-2-PHENYL TRIAZINE
  • 1,3,5-TRIAZINE-2,4-DICHLORO, 6-PHENYL-
  • 2,4-DICHLORO-6-PHENYL-1,3,5-TRIAZINE
  • 2-[(4-AMINO-3-CHLORO)BENZOYL]BENZOIC ACID
  • 2,4-Dichloro-Phenyl-1,3,5-Triazine
  • 2-Phenyl-4,6-dichlorotriazine
  • 4,6-Dichloro-2-phenyl-1,3,5-triazine
CAS:
1700-02-3
MF:
C9H5Cl2N3
MW:
226.06
EINECS:
216-928-6
Product Categories:
  • OLED
  • 1,3,5-triazine
Mol File:
1700-02-3.mol
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2,4-Dichloro-6-phenyl-1,3,5-triazine Chemical Properties

Melting point:
gt. 119.0 to 123.0 °C
Boiling point:
136°C/1mmHg(lit.)
Density 
1.428±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
-1.67±0.10(Predicted)
color 
White to Orange to Green
InChI
InChI=1S/C9H5Cl2N3/c10-8-12-7(13-9(11)14-8)6-4-2-1-3-5-6/h1-5H
InChIKey
AMEVJOWOWQPPJQ-UHFFFAOYSA-N
SMILES
N1=C(C2=CC=CC=C2)N=C(Cl)N=C1Cl
CAS DataBase Reference
1700-02-3(CAS DataBase Reference)
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Safety Information

HS Code 
2933998090
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2,4-Dichloro-6-phenyl-1,3,5-triazine Usage And Synthesis

Description

2,4-Dichloro-6-phenyl-1,3,5-triazine is a heterocyclic derivative and can be used as intermediate of synthetic materials.

Chemical Properties

White to Orange to Green powder to crystal.

Uses

2,4-Dichloro-6-phenyl-1,3,5-triazine, is a building block as an OLED intermediate for the synthesis of bipolar host materials such as 2,4,6-tris(4-(N,N-diphenylamino)phenyl)-1,3,5-triazine (TDPA–TRZ) for phosphorescent organic light-emitting diodes (PhOLED).

Synthesis

2,4-Dichloro-6-phenyl-1,3,5-triazine was prepared by reaction of 36.2 g (0.21 mol) of 2,4-dihydroxy-6-phenyl-1 ,3,5-triazine with 180 g (1.51 mol) of thionyl chloride and 17.3 g of N,N-dimethylformamide (DMF) at 60°C for 3 h. The excess thionyl chloride was distilled,and the residue was poured into water to give a product.The white product was filtered off, dried, and recrys-tallized from benzene to give a yield of 22.0 g (47.4%).

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