5-METHOXYPYRIDAZIN-3(2H)-ONE
5-METHOXYPYRIDAZIN-3(2H)-ONE Basic information
- Product Name:
- 5-METHOXYPYRIDAZIN-3(2H)-ONE
- Synonyms:
-
- 5-methoxypyridazin-3-ol
- 5-METHOXYPYRIDAZIN-3(2H)-ONE
- AURORA KA-3645
- 5-Methoxy-2,3-dihydropyridazin-3-one
- 3-hydroxy-5-Methoxypyridazine
- -METHOXYPYRIDAZIN-3(2H)-ONE
- 3-methoxy-3(2H)-pyridazinone
- 3(2H)-Pyridazinone,5-methoxy-
- CAS:
- 123696-01-5
- MF:
- C5H6N2O2
- MW:
- 126.11
- EINECS:
- 200-001-2
- Mol File:
- 123696-01-5.mol
5-METHOXYPYRIDAZIN-3(2H)-ONE Chemical Properties
- Melting point:
- 148-150 °C
- Density
- 1.30±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 10.57±0.40(Predicted)
- Appearance
- White to off-white Solid
- InChI
- InChI=1S/C5H6N2O2/c1-9-4-2-5(8)7-6-3-4/h2-3H,1H3,(H,7,8)
- InChIKey
- NRILSJUKEHQBLU-UHFFFAOYSA-N
- SMILES
- C1(=O)NN=CC(OC)=C1
5-METHOXYPYRIDAZIN-3(2H)-ONE Usage And Synthesis
Synthesis
938045-16-0
123696-01-5
General procedure for the synthesis of 5-methoxypyridazin-3(2H)-one from the compound (CAS: 938045-16-0): a mixture of 10% palladium/carbon (100 mg), 2-((benzyloxy)methyl)-4-chloro-5-methoxypyridazin-3(2H)-one (1.34 g), and acetic acid (10 mL) was subjected to a hydrogen atmosphere (0.8 MPa) with the addition of methanol (30 mL) and the reaction was stirred at 50 °C for 10 hours. After completion of the reaction, the insoluble material was removed by filtration and the solvent was removed by distillation under reduced pressure to afford the target product 5-methoxypyridazin-3(2H)-one (611 mg). Mass spectrometry analysis showed m/z (M + H): 127.
References
[1] Patent: US2015/322063, 2015, A1. Location in patent: Paragraph 2479; 2480; 2481
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5-METHOXYPYRIDAZIN-3(2H)-ONE(123696-01-5)Related Product Information
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- 6-OXO-4-PHENOXY-1-PHENYL-1,6-DIHYDRO-3-PYRIDAZINECARBOXAMIDE
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- METHYL 1-(4-METHOXYPHENYL)-6-OXO-4-PHENOXY-1,6-DIHYDRO-3-PYRIDAZINECARBOXYLATE
- 6-OXO-4-PHENOXY-1-PHENYL-1,6-DIHYDRO-3-PYRIDAZINECARBOHYDRAZIDE
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