Basic information Safety Supplier Related

2-chloro 3,5-dimethyl pyarazine

Basic information Safety Supplier Related

2-chloro 3,5-dimethyl pyarazine Basic information

Product Name:
2-chloro 3,5-dimethyl pyarazine
Synonyms:
  • 2-chloro 3,5-dimethyl pyarazine
  • 2-Chloro-3,5-dimethylpyrazine
  • 2-Chloro-3,5-dimethylpyrazine 97%
  • 2-Chloro-3,5-dimethyl-1,4-diazine
  • Pyrazine, 2-chloro-3,5-dimethyl-
CAS:
38557-72-1
MF:
C6H7ClN2
MW:
142.59
Product Categories:
  • Halides
  • Pyrazines, Pyrimidines & Pyridazines
Mol File:
38557-72-1.mol
More
Less

2-chloro 3,5-dimethyl pyarazine Chemical Properties

Boiling point:
186.6±35.0℃ (760 Torr)
Density 
1.184±0.06 g/cm3 (20 ºC 760 Torr)
refractive index 
1.5230 to 1.5270
Flash point:
83.1±11.5℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Chloroform, Methanol (Slightly)
pka
0.47±0.10(Predicted)
form 
Oil
color 
Colourless
CAS DataBase Reference
38557-72-1
More
Less

Safety Information

Risk Statements 
36/38
Safety Statements 
23-26-36/37/39
RIDADR 
1993
Hazard Note 
Harmful
HazardClass 
3
PackingGroup 
HS Code 
2933998090
More
Less

2-chloro 3,5-dimethyl pyarazine Usage And Synthesis

Uses

2-Chloro-3,5-dimethylpyrazine, is a halogenated pyrazine, that can be used as an intermediates in chemical synthesis.

Synthesis

108-50-9

38557-72-1

The general procedure for the synthesis of 2-chloro-3,5-dimethylpyrazine from 2,6-dimethylpyrazine was as follows: first, 7.12 g of 2,6-dimethylpyrazine and 6.5 mL of dimethylformamide (DMF) were added to a three-necked flask fitted with a dropping funnel and a thermometer, and refluxed under nitrogen protection. Subsequently, 6.7 mL of thionyl chloride was added to the dropping funnel and the reaction vessel was cooled in an ice bath. Thionyl chloride was slowly added dropwise while stirring the reaction mixture, controlling the reaction temperature in the range of 45 ± 5 °C. After the dropwise addition was completed, the reaction solution temperature was allowed to drop below 40°C and quenched by slowly adding water. After reconfirming that the temperature of the reaction solution was below 40 °C, aqueous sodium hydroxide was added to adjust the pH to 7-8. Subsequently, the reaction mixture was subjected to hydrodistillation. The distilled aqueous phase was extracted with dichloromethane and the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate and filtered, the filtrate was distilled to remove the solvent, and the residue was purified by distillation under reduced pressure to afford the target product 2-chloro-3,5-dimethylpyrazine (clear colorless liquid, 36% yield).

References

[1] Patent: WO2013/112788, 2013, A1. Location in patent: Paragraph 00660
[2] Patent: WO2008/149828, 2008, A1. Location in patent: Page/Page column 80-81; 82
[3] European Journal of Organic Chemistry, 2005, # 19, p. 4141 - 4153

2-chloro 3,5-dimethyl pyarazineSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Beijing Ouhe Technology Co., Ltd
Tel
010-010-82967028 13522913783
Email
2355560935@qq.com