ChemicalBook--->CAS DataBase List--->32998-25-7

32998-25-7

32998-25-7 Structure

32998-25-7 Structure
IdentificationBack Directory
[Name]

2-CHLORO-3-METHOXYQUINOXALINE
[CAS]

32998-25-7
[Synonyms]

2-CHLORO-3-METHOXYQUINOXALINE
Quinoxaline, 2-chloro-3-methoxy-
2-CHLORO-3-METHOXYQUINOXALINE ISO 9001:2015 REACH
[Molecular Formula]

C9H7ClN2O
[MDL Number]

MFCD07367979
[MOL File]

32998-25-7.mol
[Molecular Weight]

194.62
Chemical PropertiesBack Directory
[Melting point ]

71-75℃
[Boiling point ]

271℃
[density ]

1.333
[Fp ]

118℃
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-CHLORO-3-METHOXYQUINOXALINE(32998-25-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

2,3-Dichloroquinoxaline

2213-63-0

Sodium Methoxide

124-41-4

2-CHLORO-3-METHOXYQUINOXALINE

32998-25-7

To a suspension of 2,3-dichloroquinoxaline (300 mg, 1.51 mmol) in methanol (15 mL) and N,N-dimethylformamide (1.0 mL), sodium methanolate (28% methanol solution, 309 mg, 1.66 mmol) was slowly added at 0 °C. After addition, the reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the mixture was concentrated in vacuum. The residue was diluted with chloroform and water, the organic layer was separated through a partition funnel and concentrated again under vacuum. The resulting crude product was purified by silica gel column chromatography, the eluent being a gradient from pure hexane to hexane:ethyl acetate (19:1), to afford 2-chloro-3-methoxyquinoxaline (as described in Reference Example 20) as a colorless powder (251 mg, yield not provided).

[References]

[1] Patent: WO2010/30027, 2010, A1. Location in patent: Page/Page column 60
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