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19111-87-6

19111-87-6 Structure

19111-87-6 Structure
IdentificationBack Directory
[Name]

2-bromobenzo[9,10]phenanthrene
[CAS]

19111-87-6
[Synonyms]

2-bromobenzo[9
10]phenanthrene
2-BromotriphenyL
2-broMotriphenylen
2-Bromotriphenylene
2-Bromothriphenylene
Triphenylene, 2-bromo-
2-Bromotriphenylene>
2-bromobenzo[9,10]phenanthrene
[EINECS(EC#)]

807-972-2
[Molecular Formula]

C18H11Br
[MDL Number]

MFCD16659043
[MOL File]

19111-87-6.mol
[Molecular Weight]

307.184
Chemical PropertiesBack Directory
[Melting point ]

132.0 to 136.0 °C
[Boiling point ]

482.9±14.0 °C(Predicted)
[density ]

1.477
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO, Methanol (Slightly, Heated)
[form ]

Solid
[color ]

Pale Beige
[InChI]

InChI=1S/C18H11Br/c19-12-9-10-17-15-7-2-1-5-13(15)14-6-3-4-8-16(14)18(17)11-12/h1-11H
[InChIKey]

GEDOYYDMCZUHNW-UHFFFAOYSA-N
[SMILES]

C1=C2C(C3C(C4C2=CC=CC=4)=CC=CC=3)=CC=C1Br
[Odor]

White to off-white powder
Questions And AnswerBack Directory
[Uses]

2-Bromobenzo[9,10]phenanthrene is a useful research chemical.
Hazard InformationBack Directory
[Description]

2-Bromotriphenylene, also known as 2-bromobenzo[9,10]phenanthrene, is an OLED intermediate for the synthesis of hole transport layer (HTL) materials or host materials. It is electron rich and has a planar structure in electroluminescence devices.
[Chemical Properties]

white to off-white solid
[Synthesis]

Triphenylene

217-59-4

2-bromobenzo[9,10]phenanthrene

19111-87-6

The general procedure for the synthesis of 2-bromobenzo[9,10]phenanthrene from 9,10-benzo[9,10]phenanthrene was as follows (Example 1, Synthesis of Compounds A-8): (1) Synthesis of compound d-2: Add compound d-1 (9.99 g, 43.8 mmol) and dichloromethane (300 mL) in a 500 mL three-neck flask. The reaction solution was stirred at room temperature under nitrogen protection and a mixed solution consisting of bromine (7.7 g, 48.2 mmol) and dichloromethane (7.0 mL) was added slowly dropwise. After the dropwise addition, the reaction solution was continued to be stirred at room temperature for 12 hours. Upon completion of the reaction, the reaction solution was quenched by pouring it into sodium thiosulfate solution. Subsequently, the organic layer was extracted with chloroform, combined and dried with anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to obtain the crude product. Finally, the crude product was purified by silica gel column chromatography (unfolding agent: toluene-heptane mixed solvent) to afford 11.6 g of compound d-2 as a white solid (yield: 86.3%).

[References]

[1] Patent: WO2012/86366, 2012, A1. Location in patent: Page/Page column 23-24
[2] Patent: CN105431441, 2016, A. Location in patent: Paragraph 0147; 0148; 0149
[3] Journal of the Chemical Society, 1955, p. 4482,4484
[4] Patent: WO2009/21107, 2009, A1. Location in patent: Page/Page column 31
[5] Patent: WO2009/37155, 2009, A1. Location in patent: Page/Page column 65-66
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[HS Code ]

2902900000
Spectrum DetailBack Directory
[Spectrum Detail]

2-bromobenzo[9,10]phenanthrene(19111-87-6)1HNMR
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