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2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINE

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2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINE Basic information

Product Name:
2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINE
Synonyms:
  • 2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINE
  • IMidazo[1,2-b]pyridazine,2,6-dichloro-
  • 2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINE ISO 9001:2015 REACH
CAS:
112581-77-8
MF:
C6H3Cl2N3
MW:
188.01
Mol File:
112581-77-8.mol
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2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINE Chemical Properties

Density 
1.69
storage temp. 
2-8°C
InChI
InChI=1S/C6H3Cl2N3/c7-4-1-2-6-9-5(8)3-11(6)10-4/h1-3H
InChIKey
MGNCSIAIZSTMHX-UHFFFAOYSA-N
SMILES
C12=NC(Cl)=CN1N=C(Cl)C=C2
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Safety Information

HS Code 
2933998090
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2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINE Usage And Synthesis

Synthesis

127566-18-1

112581-77-8

Example 4: 1.88 g of 6-chloro-3-imino-2,3-dihydropyridazine-2-acetic acid (purity: 99.5 wt%) was mixed with 7.52 g of monochlorobenzene and 0.79 g of pyridine. 3.84 g of phosphoryl chloride was slowly added dropwise to the mixture over a period of 3 minutes at an endothermic condition of 20 to 40 °C. Subsequently, the reaction system was heated to an endothermic temperature of 120 °C within 20 minutes and the reaction was continued at this temperature for 6 hours. Upon completion of the reaction, the mixture was cooled to give a reaction mixture containing 2,6-dichloroimidazo[1,2-b]pyridazine.The yield of 2,6-dichloroimidazo[1,2-b]pyridazine was 99%.

References

[1] Patent: EP1930331, 2008, A1. Location in patent: Page/Page column 5
[2] Patent: EP1930331, 2008, A1. Location in patent: Page/Page column 4
[3] Patent: EP1930331, 2008, A1. Location in patent: Page/Page column 4
[4] Patent: EP1930331, 2008, A1. Location in patent: Page/Page column 5
[5] Patent: EP1930331, 2008, A1. Location in patent: Page/Page column 5

2,6-DICHLOROIMIDAZO[1,2-B]PYRIDAZINESupplier

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