ChemicalBook--->CAS DataBase List--->4774-15-6

4774-15-6

4774-15-6 Structure

4774-15-6 Structure
IdentificationMore
[Name]

2,6-Dimethoxypyrazine
[CAS]

4774-15-6
[Synonyms]

2,6-DIMETHOXYPYRAZINE
2,6-DIMETHOXYPYRAZINE,99+%
[Molecular Formula]

C6H8N2O2
[MDL Number]

MFCD00955843
[Molecular Weight]

140.14
[MOL File]

4774-15-6.mol
Chemical PropertiesBack Directory
[Melting point ]

31-31.5 °C
[Boiling point ]

75 °C(Press: 10 Torr)
[density ]

1.131
[refractive index ]

1.49
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

0.15±0.10(Predicted)
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

4774-15-6(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

2,6-Dimethoxypyrazine(4774-15-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,6-Dichloropyrazine

4774-14-5

Sodium Methoxide

124-41-4

2,6-Dimethoxypyrazine

4774-15-6

Synthesis of 2,6-dimethoxypyrazine (V): a mixture of 2,6-dichloropyrazine (3.9 g, 26 mmol) with freshly prepared sodium methanol (62 mmol) in anhydrous methanol (50 ml) was heated to reflux overnight. After completion of the reaction, the solvent was removed under reduced pressure. The residue was diluted to 100 ml with dichloromethane (CH2Cl2), washed sequentially with water and saturated saline, then dried over anhydrous magnesium sulfate (MgSO4) and filtered. The filtrate was concentrated by evaporation under reduced pressure to give pure 2,6-dimethoxypyrazine (V) (3.6 g, 98% yield) as colorless crystals. Its 1H NMR (CDCl3) data were as follows: δ 3.94 (s, 6H); 7.76 (s, 2H).

[References]

[1] Tetrahedron, 2009, vol. 65, # 43, p. 8891 - 8895
[2] Patent: WO2008/70908, 2008, A1. Location in patent: Page/Page column 76-77
[3] Asian Journal of Chemistry, 2013, vol. 25, # 9, p. 4979 - 4982
[4] Journal of Heterocyclic Chemistry, 2016, vol. 53, # 5, p. 1386 - 1394
[5] Journal of the Chemical Society, 1965, p. 6681,6686
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