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4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE

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4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE Basic information

Product Name:
4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE
Synonyms:
  • 4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE
  • AURORA KA-6685
  • 4-Chloro-2,3-dihydro-5-methoxy-3-oxopyridazine
  • 5-chloro-4-methoxy-1H-pyridazin-6-one
  • 4-Chloro-5-methoxy-3(2H)-pyridazinone
  • 4-chloro-5-methoxy-2,3-dihydropyridazin-3-one
  • 3(2H)-Pyridazinone, 4-chloro-5-methoxy-
  • 4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE ISO 9001:2015 REACH
CAS:
63910-43-0
MF:
C5H5ClN2O2
MW:
160.56
Product Categories:
  • Pyrazines, Pyrimidines & Pyridazines
  • Pyrazines, Pyrimidines & Pyridazines
Mol File:
63910-43-0.mol
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4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE Chemical Properties

Melting point:
225 °C(dec.)
Density 
1.51±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
8.90±0.60(Predicted)
color 
White to Orange to Green
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Safety Information

HS Code 
2933399990
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4-CHLORO-5-METHOXYPYRIDAZIN-3(2H)-ONE Usage And Synthesis

Synthesis

932-22-9

124-41-4

63910-43-0

General procedure for the synthesis of 4-chloro-5-methoxypyridazin-3(2H)-one (10): to a solution of 4,5-dichloropyridazin-3(2H)-one (4.1 g, 24.8 mmol) in methanol (50 mL) was added sodium methanolate (2.6 g, 74.5 mmol). The reaction mixture was stirred at 80 °C overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and purified by column chromatography [eluent: petroleum ether to petroleum ether/dichloromethane/methanol (10:1:1)] to afford the target product, 4-chloro-5-methoxypyridazin-3(2H)-one (10) (1.2 g, 30% yield), as a white solid. The procedure for the synthesis of 4-chloro-2-(2-chlorobenzyl)-5-methoxypyridazin-3(2H)-one (11) was not provided with complete information.

References

[1] Journal of Medicinal Chemistry, 2004, vol. 47, # 19, p. 4716 - 4730
[2] Patent: WO2015/143164, 2015, A1. Location in patent: Page/Page column 115
[3] Monatshefte fuer Chemie, 1989, vol. 120, p. 329 - 342

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