ChemicalBook--->CAS DataBase List--->57339-57-8

57339-57-8

57339-57-8 Structure

57339-57-8 Structure
IdentificationBack Directory
[Name]

6-bromoquinolin-8-amine
[CAS]

57339-57-8
[Synonyms]

6-bromoquinolin-8-amine
6-Bromo-8-quinolinamine
6-BroMo-8-aMinoquinoline
8-QuinolinaMine, 6-broMo-
[Molecular Formula]

C9H7BrN2
[MDL Number]

MFCD00194777
[MOL File]

57339-57-8.mol
[Molecular Weight]

223.07
Chemical PropertiesBack Directory
[Melting point ]

78 °C
[Boiling point ]

370.4±27.0 °C(Predicted)
[density ]

1.649±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

2.22±0.10(Predicted)
[Appearance]

Light green to green Solid
[EPA Substance Registry System]

8-Quinolinamine, 6-bromo- (57339-57-8)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H332
[Precautionary statements ]

P280
[TSCA ]

TSCA listed
[HS Code ]

2933499090
Spectrum DetailBack Directory
[Spectrum Detail]

6-bromoquinolin-8-amine(57339-57-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-bromo-8-nitroquinoline

68527-67-3

6-bromoquinolin-8-amine

57339-57-8

General procedure for the synthesis of 6-bromo-8-aminoquinoline from 6-bromo-8-nitroquinoline: to a mixed solution of 6-bromo-8-nitroquinoline (4 g, 1.58 mmol) in ethanol/acetic acid/water (50 mL/50 mL/25 mL) was added iron powder (3.18 g, 5.69 mmol). The reaction mixture was heated to reflux for 3 hours. Upon completion of the reaction, it was cooled to room temperature, neutralized with 2.5 N sodium hydroxide solution, filtered through diatomaceous earth to remove the iron powder residue, and the filter cake was washed with ethyl acetate. The filtrate was extracted with ethyl acetate (3 x 200 mL), the organic phases were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure. The oil obtained was purified by column chromatography (40% ethyl acetate/hexane) to give 3.19 g (91% yield) of yellow solid with a melting point of 142-145 °C. The residue was extracted with ethyl acetate (3 x 200 mL) and dried with anhydrous sodium sulfate.

[References]

[1] Patent: EP1147083, 2004, B1. Location in patent: Page 46
[2] Monatshefte fuer Chemie, 1994, vol. 125, # 6/7, p. 723 - 730
[3] Journal fuer Praktische Chemie (Leipzig), 1894, vol. <2> 49, p. 534,539
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