ChemicalBook--->CAS DataBase List--->13438-50-1

13438-50-1

13438-50-1 Structure

13438-50-1 Structure
IdentificationBack Directory
[Name]

3-BROMOFLUORANTHENE
[CAS]

13438-50-1
[Synonyms]

3-BROMOFLUORANTHENE
Fluoranthene, 3-?bromo-
3-Bromofluoranthene >
[EINECS(EC#)]

808-043-4
[Molecular Formula]

C16H9Br
[MDL Number]

MFCD07787460
[MOL File]

13438-50-1.mol
[Molecular Weight]

281.15
Chemical PropertiesBack Directory
[Melting point ]

106.0 to 200.0 °C
[Boiling point ]

207°C/0.2mmHg(lit.)
[density ]

1.578±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly)
[form ]

Solid
[color ]

Light Yellow to Yellow
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 ]

2902900000
Hazard InformationBack Directory
[Uses]

3-Bromofluoranthene is an intermediate in synthesizing 3-Methylfluoranthene (M305315), an environmental pollutant that is an active tumor initiator.
[Synthesis]

Fluoranthene

206-44-0

3-BROMOFLUORANTHENE

13438-50-1

Preparation of Compound 2-1: 50 g (247 mmol) of fluoranthene was dissolved in 1 L of nitrobenzene, and a dilute solution consisting of 12 mL (234.7 mmol) of bromine and 200 mL of nitrobenzene was added slowly and dropwise. After the dropwise addition, the reaction mixture was stirred at room temperature for 20 hours. Upon completion of the reaction, 500 mL of saturated aqueous sodium thiosulfate solution was added to quench the reaction. The reaction mixture was extracted with 3 L of ethyl acetate, followed by washing the organic phase with 1 L of distilled water. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was filtered through silica gel column and purified by recrystallization to give the final compound 2-1 (65 g, 94% yield).

[References]

[1] Patent: WO2012/30145, 2012, A1. Location in patent: Page/Page column 15-16
[2] Patent: WO2013/32278, 2013, A1. Location in patent: Paragraph 94; 95
[3] Patent: KR2016/64432, 2016, A. Location in patent: Paragraph 0089-0091
[4] Journal of the American Chemical Society, 1966, vol. 88, # 24, p. 5837 - 5845
[5] Patent: US2011/34744, 2011, A1. Location in patent: Page/Page column 24
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMOFLUORANTHENE(13438-50-1)1HNMR
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