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1700-02-3

1700-02-3 Structure

1700-02-3 Structure
IdentificationMore
[Name]

2,4-Dichloro-6-phenyl-1,3,5-triazine
[CAS]

1700-02-3
[Synonyms]

1,3,5-TRIAZINE-2,4-DICHLORO, 6-PHENYL-
2-[(4-AMINO-3-CHLORO)BENZOYL]BENZOIC ACID
2,4-DICHLORO-6-PHENYL-1,3,5-TRIAZINE
4,6-DICHLORO-2-PHENYL TRIAZINE
LABOTEST-BB LT00044422
2,4-Dichloro-Phenyl-1,3,5-Triazine
2-Phenyl-4,6-dichlorotriazine
4,6-Dichloro-2-phenyl-1,3,5-triazine
6-PHENYL-1,3,5-TRIAZINE-2,4-DICHLORO
[EINECS(EC#)]

216-928-6
[Molecular Formula]

C9H5Cl2N3
[MDL Number]

MFCD00602464
[Molecular Weight]

226.06
[MOL File]

1700-02-3.mol
Chemical PropertiesBack Directory
[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)
[Description]

PTRZ-2Cl, namely 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).
[Odor]

White to off-white powder
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
[HS Code ]

2933998090
Hazard InformationBack Directory
[Chemical Properties]

White to Orange to Green powder to crystal.
[Uses]

2,4-Dichloro-6-phenyl-1,3,5-triazine is a heterocyclic derivative and can be used as intermediate of synthetic materials.
[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%).
1700-02-3.png
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-Dichloro-6-phenyl-1,3,5-triazine(1700-02-3)1HNMR
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