ChemicalBook--->CAS DataBase List--->552331-06-3

552331-06-3

552331-06-3 Structure

552331-06-3 Structure
IdentificationBack Directory
[Name]

6-BROMO-3-CHLOROISOQUINOLINE
[CAS]

552331-06-3
[Synonyms]

6-BROMO-3-CHLOROISOQUINOLINE
Isoquinoline, 6-bromo-3-chloro-
6-Bromo-3-chloro-2-azanaphthalene
6-bromanyl-3-chloranyl-isoquinoline
6-BROMO-3-CHLOROISOQUINOLINE ISO 9001:2015 REACH
[Molecular Formula]

C9H5BrClN
[MDL Number]

MFCD08703290
[MOL File]

552331-06-3.mol
[Molecular Weight]

242.5
Chemical PropertiesBack Directory
[Boiling point ]

349.5±22.0 °C(Predicted)
[density ]

1.673±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[form ]

solid
[pka]

1.28±0.38(Predicted)
[color ]

Pale yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319
[Precautionary statements ]

P305+P351+P338
[Hazard Codes ]

Xn
[Risk Statements ]

22
[HS Code ]

2933499090
Spectrum DetailBack Directory
[Spectrum Detail]

6-BROMO-3-CHLOROISOQUINOLINE(552331-06-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-Bromo-1,3-dichloroisoquinoline

552331-05-2

6-BROMO-3-CHLOROISOQUINOLINE

552331-06-3

General procedure for the synthesis of 6-bromo-3-chloroisoquinoline from 6-bromo-1,3-dichloroisoquinoline: a mixture of 6-bromo-1,3-dichloroisoquinoline (1.8 g, 6.5 mmol), red phosphorus (0.48 g, 15.5 mmol), and hydriodic acid (3 ml, 48%) in acetic acid (20 ml) was heated and refluxed for 8 hours. After completion of the reaction, it was filtered while hot and the filtrate was concentrated under reduced pressure. The concentrated residue was alkalized by addition of sodium hydroxide solution and subsequently extracted with ethyl acetate (200 mL). The organic phase was washed with saturated saline, dried over anhydrous magnesium sulfate, filtered and concentrated. The concentrate was purified by silica gel fast column chromatography to afford 6-bromo-3-chloroisoquinoline (0.81 g, 50% yield) using 30% ethyl acetate/hexane as eluent. Mass spectrum (DCI/NH3) m/e 244 (M+H)+.

[References]

[1] Patent: US2003/187026, 2003, A1
[2] Patent: US2003/199511, 2003, A1. Location in patent: Page/Page column 34-35
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