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204530-94-9

204530-94-9 Structure

204530-94-9 Structure
IdentificationBack Directory
[Name]

1-(4-Bromophenyl)-naphthlene
[CAS]

204530-94-9
[Synonyms]

1-(4-BroMophenyl)phthalene
1-(4-bromophenyl)naphthalen
1-(4-BROMOPHENYL)-NAPHTHLENE
Naphthalene, 1-(4-bromopheny)-
1-(4-Bromophenyl)naphthalene>
Naphthalene, 1-(4-bromophenyl)-
1-(4-Bromophenyl)-naphthalene ,97%
[EINECS(EC#)]

812-991-4
[Molecular Formula]

C16H11Br
[MDL Number]

MFCD07369916
[MOL File]

204530-94-9.mol
[Molecular Weight]

283.16
Chemical PropertiesBack Directory
[Melting point ]

75-76 °C
[Boiling point ]

381.6±11.0 °C(Predicted)
[density ]

1.381±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

soluble in Toluene
[form ]

yellow oil
[color ]

White to Almost white
[InChI]

InChI=1S/C16H11Br/c17-14-10-8-13(9-11-14)16-7-3-5-12-4-1-2-6-15(12)16/h1-11H
[InChIKey]

YRPIGRRBBMFFBE-UHFFFAOYSA-N
[SMILES]

C1(C2=CC=C(Br)C=C2)=C2C(C=CC=C2)=CC=C1
Questions And AnswerBack Directory
[Uses]

1-(4-bromophenyl)naphthalene is an aromatic hydrocarbon derivative that can be used as an organic optoelectronic intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HS Code ]

2903998090
Hazard InformationBack Directory
[Chemical Properties]

off-white powder
[Synthesis]

1-Bromo-4-iodobenzene

589-87-7

1-Naphthylboronic acid

13922-41-3

1-(4-Bromophenyl)-naphthlene

204530-94-9

Under argon protection, 1-naphthaleneboronic acid (200.0 g, 1.163 mol), 4-bromoiodobenzene (329.0 g, 1.163 mol), tetrakis(triphenylphosphine)palladium(0) (26.9 g, 23.3 mmol), toluene (3.7 L), and 2M aqueous sodium carbonate (1.74 L) were added to the reaction vessel. The reaction mixture was stirred at 90 °C for 24 hours. After completion of the reaction, the mixture was filtered to remove the aqueous phase. The organic phase was washed with water and subsequently dried with magnesium sulfate. The toluene solvent was removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography to afford 1-(4-bromophenyl)naphthalene (268 g, 81% yield).

[References]

[1] Patent: US2010/331585, 2010, A1. Location in patent: Page/Page column 96
[2] Patent: KR2017/49295, 2017, A. Location in patent: Paragraph 0137-0142
[3] Patent: WO2008/13399, 2008, A1. Location in patent: Page/Page column 15
[4] Patent: US9419237, 2016, B2. Location in patent: Page/Page column 65; 66
[5] Patent: KR2015/38093, 2015, A. Location in patent: Paragraph 0476-0481
Spectrum DetailBack Directory
[Spectrum Detail]

1-(4-Bromophenyl)-naphthlene(204530-94-9)1HNMR
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