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2-Chloro-6-methylpyrazine

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2-Chloro-6-methylpyrazine Basic information

Product Name:
2-Chloro-6-methylpyrazine
Synonyms:
  • 2-Chloro-6-methylpyrazine 97%
  • 2-Methyl-6-chloropyrazine
  • 6-Methyl-2-chloropyrazine
  • 2-Chloro-6-methylpyrazine, >=98%
  • 2-Chloro-6-methylpyrazine97%
  • 2-CHLORO-6-METHYLPYRAZINE
  • 2-Chloro-6-methyl-1,4-diazine
  • 2-Chloro-6-methylpyrazine >
CAS:
38557-71-0
MF:
C5H5ClN2
MW:
128.56
Product Categories:
  • Halides
  • Pyrazines, Pyrimidines & Pyridazines
  • Pyrazines, Pyrimidines & Pyridazines
Mol File:
38557-71-0.mol
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2-Chloro-6-methylpyrazine Chemical Properties

Melting point:
49-52
Boiling point:
83°C/35mmHg(lit.)
Density 
1.234±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
-0.89±0.10(Predicted)
color 
White to Almost white
InChIKey
CKUVSPQGYLELRG-UHFFFAOYSA-N
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
20/21/22-36/37/38-22
Safety Statements 
22-26-36/37/39
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29339900
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2-Chloro-6-methylpyrazine Usage And Synthesis

Chemical Properties

Solid

Uses

2-Chloro-6-methylpyrazine was used in the synthesis of palm site inhibitors of HCV NS5B polymerase and potent dipeptidyl peptidase IV inhibitors.

Synthesis

930798-25-7

38557-71-0

Step 3: To a 5L sealed reaction tube was added (6-chloropyrazin-2-yl)acetic acid (220 g, 1.27 mol, 1.00 equiv) and deionized water (3L). The reaction mixture was stirred at 130 °C overnight. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently extracted with ether (2 x 3 L). The organic phases were combined, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford 238 g (73% yield) of 2-chloro-6-methylpyrazine as a yellow solid.

References

[1] Patent: US2015/31674, 2015, A1. Location in patent: Paragraph 0325; 0322

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