Basic information Safety Supplier Related

8-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE

Basic information Safety Supplier Related

8-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE Basic information

Product Name:
8-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE
Synonyms:
  • 8-CHLOROTRIAZOLO[4,3-A]PYRAZINE
  • 8-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE
  • 1,2,4-Triazolo[4,3-a]pyrazine,8-chloro-
  • 8-Chloro-1,2,4-triazolo[4,3-a]pyrazine,97%
  • 8-Chloro-1,2,4-triazolo[4,3-a]pyrazine
CAS:
68774-77-6
MF:
C5H3ClN4
MW:
154.56
Mol File:
68774-77-6.mol
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8-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE Chemical Properties

Melting point:
215-220℃
Density 
1.71±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1.10±0.30(Predicted)
form 
Solid
color 
Brown
InChIKey
VKZJRJVVFDDJKP-UHFFFAOYSA-N
CAS DataBase Reference
68774-77-6
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/37/38
Safety Statements 
26
WGK Germany 
3
HS Code 
2933998090
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8-CHLORO-[1,2,4]TRIAZOLO[4,3-A]PYRAZINE Usage And Synthesis

Synthesis

122-51-0

63286-28-2

68774-77-6

Using 2-chloro-3-hydrazinopyrazine (8 g) and triethyl orthoformate (32 mL), the mixture was heated to reflux and stirred for 4 hours. Upon completion of the reaction, the reaction solution was cooled to room temperature, the precipitated solid was collected by filtration and washed with ethanol. The resulting solid was 8-chloro-[1,2,4]triazolo[4,3-A]pyrazine, which was dried under reduced pressure to give the product (8.10 g, 95% yield).

References

[1] Patent: JP5851663, 2016, B1. Location in patent: Paragraph 0301
[2] Patent: WO2009/64418, 2009, A1. Location in patent: Page/Page column 85
[3] Patent: US2010/120774, 2010, A1. Location in patent: Page/Page column 37-38

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