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23449-08-3

23449-08-3 Structure

23449-08-3 Structure
IdentificationBack Directory
[Name]

2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine
[CAS]

23449-08-3
[Synonyms]

PTZ-Br
)-4,6-diphenyL
2-(4-bromophenyl)-4
1,3,5-Triazine, 2-(4-bromopheny)-4,6-dipheny-
2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine
1,3,5-Triazine, 2-(4-broMophenyl)-4,6-diphenyl-
[Molecular Formula]

C21H14BrN3
[MDL Number]

MFCD00194632
[MOL File]

23449-08-3.mol
[Molecular Weight]

388.26
Chemical PropertiesBack Directory
[Melting point ]

200.0 to 204.0 °C
[Boiling point ]

573.9±52.0 °C(Predicted)
[density ]

1.381
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

powder to crystal
[pka]

0.45±0.10(Predicted)
[color ]

White to Almost white
[InChI]

InChI=1S/C21H14BrN3/c22-18-13-11-17(12-14-18)21-24-19(15-7-3-1-4-8-15)23-20(25-21)16-9-5-2-6-10-16/h1-14H
[InChIKey]

AYHGAQGOMUQMTR-UHFFFAOYSA-N
[SMILES]

N1=C(C2=CC=CC=C2)N=C(C2=CC=CC=C2)N=C1C1=CC=C(Br)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

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

29336990
Hazard InformationBack Directory
[Chemical Properties]

white solid powder
[Uses]

2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine serves as a reactant in the synthesis of 2,4-diphenyl-6-(4'-triphenylsilanyl-biphenyl-4-yl)-1,3,5-triazine (DTBT) via coupling with 4-phenylboronic acid triphenylsilane, using tetrakis(triphenylphosphine)palladium(0) and potassium carbonate in toluene under nitrogen at 110 °C[6].
[Synthesis]

The compound, 2-chloro-4,6-diphenyl-1,3,5-triazine (50 g, 187 mmol) was dissolved in THF (1 L) under a nitrogen environment, (4-bromophenyl)boronic acid (45 g, 224.12 mmol, Aldrich Corporation), and tetrakis(triphenylphosphine)palladium (2.1 g, 1.87 mmol) were added thereto, and the mixture was stirred. Potassium carbonate saturated in water (64 g, 467 mmol) was added thereto, and the obtained mixture was heated and refluxed at 80° C. for 12 hours. When the reaction was complete, water was added to the reaction solution, and the mixture was extracted with dichloromethane (DCM) and then, filtered after removing moisture with anhydrous MgSO4 and concentrated under a reduced pressure. This obtained residue was separated and purified through flash column chromatography to obtain 2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine (70 g and 96%).
[References]

[1] Patent: US2017/331067, 2017, A1. Location in patent: Paragraph 0260-0263
[2] Chemistry - An Asian Journal, 2016, vol. 11, # 6, p. 868 - 873
[3] Patent: KR2015/75169, 2015, A. Location in patent: Paragraph 0206-0209
[4] Patent: KR2015/59395, 2015, A. Location in patent: Paragraph 0162; 0163; 0164; 0165
[5] Patent: KR2015/88163, 2015, A. Location in patent: Paragraph 0342-0345
Spectrum DetailBack Directory
[Spectrum Detail]

2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine(23449-08-3)MS
2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine(23449-08-3)1HNMR
2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine(23449-08-3)IR1
2-(4-bromophenyl)-4,6-diphenyl-1,3,5-triazine(23449-08-3)IR2
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