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27825-21-4

27825-21-4 Structure

27825-21-4 Structure
IdentificationBack Directory
[Name]

METHYL 3-CHLORO-2-PYRAZINECARBOXYLATE
[CAS]

27825-21-4
[Synonyms]

3-Chloro-pyrazine-2-carbo...
METHYL 3-CHLORO-2-PYRAZINECARBOXYLATE
Methyl 3-chloropyrazine-2-car boxylate
3-chloro-5-Methylpyrazine-2-carboxylate
Methyl3-Chloropyrazine-2-carboxylate>
Methyl 3-chloropyrazine-2-carboxylate, 97+%
3-Chloro-2-pyrazinecarboxylic Acid Methyl Ester
Pyrazinecarboxylic acid, 3-chloro-, methyl ester
3-chloro-pyrazine-2-carboxylic acid methyl ester
2-Pyrazinecarboxylic acid, 3-chloro-, methyl ester
METHYL 3-CHLORO-2-PYRAZINECARBOXYLATE ISO 9001:2015 REACH
[Molecular Formula]

C6H5ClN2O2
[MDL Number]

MFCD03093326
[MOL File]

27825-21-4.mol
[Molecular Weight]

172.57
Chemical PropertiesBack Directory
[Melting point ]

31-32 °C
[Boiling point ]

89°C/2mmHg(lit.)
[density ]

1.372±0.06 g/cm3(Predicted)
[storage temp. ]

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

powder to lump
[pka]

-2.33±0.10(Predicted)
[color ]

White to Orange to Green
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Flame (GHS02)
GHS05,GHS02
[Signal word ]

Danger
[Hazard statements ]

H314-H225-H290
[Precautionary statements ]

P501-P240-P210-P233-P234-P243-P241-P242-P264-P280-P370+P378-P390-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P403+P235-P406-P405
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

3-Chloro-2-pyrazinecarboxylic Acid Methyl Ester (cas# 27825-21-4) is a compound useful in organic synthesis.
[Synthesis]

Methanol

67-56-1

3-CHLORO-2-PYRAZINE-CARBOXYLIC ACID

27398-39-6

METHYL 3-CHLORO-2-PYRAZINECARBOXYLATE

27825-21-4

General procedure for the synthesis of methyl 3-chloro-2-pyrazinecarboxylate from methanol and 2-chloropyrazine-3-carboxylic acid: 3-chloropyrazine-2-carboxylic acid (100 mg, 0.63 mmol) was dissolved in a solvent mixture (2 mL : 2 mL) of dichloromethane (DCM) and methanol (MeOH) at room temperature. To this solution was added trimethylsilyl diazomethane (TMSCHN2, 0.47 mL, 0.95 mmol). The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of acetic acid (0.2 mL) and the reaction mixture was diluted with distilled water (2 mL). Subsequently, the aqueous phase was extracted with dichloromethane (4 mL × 3). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford methyl 3-chloro-2-pyrazinecarboxylate (100 mg) as a colorless oil. Analyzed by liquid chromatography-mass spectrometry (LRMS), the molecular ion peak m/z (M + H) was measured to be 173.0, which was consistent with the theoretical value of 173.0.

[References]

[1] Patent: WO2016/100157, 2016, A2. Location in patent: Page/Page column 54; 55
[2] Patent: WO2016/101119, 2016, A1. Location in patent: Page/Page column 42; 43
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 3-CHLORO-2-PYRAZINECARBOXYLATE(27825-21-4)1HNMR
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