ChemicalBook--->CAS DataBase List--->625854-02-6

625854-02-6

625854-02-6 Structure

625854-02-6 Structure
IdentificationBack Directory
[Name]

9-(4-broMophenyl)-10-phenylanthracene
[CAS]

625854-02-6
[Synonyms]

9-(4-broMophenyl)-10-phenylanthracene
9-phenyl-10-(4-bromophenyl)anthracene
Anthracene, 9-(4-bromophenyl)-10-phenyl-
9-(4-Bromophenyl)-10-phenylanthracene >
9-(4-broMophenyl)-10-phenylanthracene ISO 9001:2015 REACH
[Molecular Formula]

C26H17Br
[MDL Number]

MFCD24842536
[MOL File]

625854-02-6.mol
[Molecular Weight]

409.317
Questions And AnswerBack Directory
[Uses]

9-(4-Bromophenyl)-10-phenylanthracene (cas# 625854-02-6) is a useful research chemical.
Chemical PropertiesBack Directory
[Melting point ]

225.0 to 229.0 °C
[Boiling point ]

505.4±19.0 °C(Predicted)
[density ]

1.344±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

slightly sol. in Toluene
[form ]

powder to crystal
[color ]

White to Light yellow to Green
[CAS DataBase Reference]

625854-02-6
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335-H412
[Precautionary statements ]

P261-P273-P305+P351+P338
[HS Code ]

2903998090
Spectrum DetailBack Directory
[Spectrum Detail]

9-(4-broMophenyl)-10-phenylanthracene(625854-02-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Bromophenylboronic acid

5467-74-3

Anthracene, 9-iodo-10-phenyl-

150712-74-6

9-(4-broMophenyl)-10-phenylanthracene

625854-02-6

The general procedure for the synthesis of 9-(4-bromophenyl)-10-phenylanthracene from 4-bromophenylboronic acid and compound (CAS:150712-74-6) is as follows: (iv) Synthesis of 9-(4-bromophenyl)-10-phenylanthracene In a 100 mL three-necked flask, 5.3 g (14 mmol) of 9-iodo-10-phenylanthracene, 2.9 g (14 mmol) of 4-bromophenylboronic acid and 0.18 g (0.15 mmol) of tetrakis(triphenylphosphine)palladium(0) were added sequentially. Subsequently, the atmosphere in the flask was replaced with nitrogen. To the reaction system was added 30 mL of toluene and 15 mL (31 mmol) of 2.0 mol/L aqueous sodium carbonate solution. The mixture was reacted at reflux for 10 h at 110 °C. Upon completion of the reaction, the precipitate in the reaction mixture was collected by diafiltration. The resulting solid was dissolved in toluene and filtered sequentially by filtration through Florisil, diatomaceous earth and alumina. The filtrate was concentrated and the resulting solid was recrystallized using a solvent mixture of chloroform and hexane. The final 4.1 g of the target product, 9-(4-bromophenyl)-10-phenylanthracene, was obtained as a light yellow powdery solid in 72% yield. The following is the synthetic scheme of 9-(4-bromophenyl)-10-phenylanthracene (synthetic scheme b-4).

[References]

[1] Patent: US2008/81934, 2008, A1. Location in patent: Page/Page column 36
[2] Patent: WO2006/104221, 2006, A1. Location in patent: Page/Page column 61-62
[3] Patent: WO2007/13537, 2007, A1. Location in patent: Page/Page column 95-96
[4] Patent: WO2007/7885, 2007, A1. Location in patent: Page/Page column 54
[5] Patent: US2007/96639, 2007, A1. Location in patent: Page/Page column 111
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