| Identification | Back Directory |  [Name]
  6-HYDROXY-3-PYRIDAZINECARBOXYLIC ACID MONOHYDRATE |  [CAS]
  37972-69-3 |  [Synonyms]
  3-hydroxypyridazine-6-car... 6-Carboxy-3(2H)-pyridazinone 1,6-dihydro-6-ox-3-darbazinate 6-Hydroxy-3-pyridazinecarboxylic acid 4-hydroxypyriMidine-2-carboxylic acid 6-oxo-1H-pyridazine-3-carboxylic acid 6-keto-1H-pyridazine-3-carboxylic acid 6-hydroxy-pyridazine-3-carboxylic acid 6-Hydroxypyridazine-3-carboxylic acid 98% 1,6-Dihydro-6-oxo-3-pyridazinecarboxylic acid 6-Oxo-1,6-dihydropyridazine-3-carboxylic acid 3-Pyridazinecarboxylic acid, 1,6-dihydro-6-oxo- 6-Hydroxy-3-pyridazinecarboxylic acid monohydrate 2,3-DIHYDRO-3-OXOPYRIDAZIN-6-CARBOXYLIC ACID, MONOHYDRATE 6-oxo-1,6-dihydropyridazine-3-carboxylic acid(SALTDATA: FREE) |  [EINECS(EC#)]
  675-237-1 |  [Molecular Formula]
  C5H6N2O4 |  [MDL Number]
  MFCD00052805 |  [MOL File]
  37972-69-3.mol |  [Molecular Weight]
  158.112 |  
 | Chemical Properties | Back Directory |  [Melting point ]
  246 °C |  [density ]
  1.63±0.1 g/cm3(Predicted) |  [storage temp. ]
  Sealed in dry,Room Temperature |  [pka]
  -2.86±0.20(Predicted) |  [Appearance]
  White to yellow Solid |  
 | Hazard Information | Back Directory |  [Uses]
  6-Hydroxypyridazine-3-carboxylic acid is a carboxylic acid derivative and can be used as an intermediate in organic synthesis. |  [Synthesis]
 
 The general procedure for the synthesis of 6-hydroxypyridazine-3-carboxylic acid from 6-oxo-1,4,5,6-tetrahydropyridazine-3-carboxylic acid was as follows: to a solution of 6-oxo-1,4,5,6-tetrahydropyridazine-3-carboxylic acid (2.50 g, 17.59 mmol) in toluene (44 mL) was added sequentially copper acetate (450 mg, 2.48 mmol), sodium carbonate ( 7.01 g, 66.14 mmol) and pyridine (4.4 mL). The reaction mixture was stirred and mixed at room temperature, then warmed to 100 °C and stirred continuously for 16 hours. After completion of the reaction, the insoluble solid was removed by filtration and the filtrate was concentrated under reduced pressure to afford 6-oxo-1,6-dihydropyridazine-3-carboxylic acid as an off-white solid (1.80 g, 73% yield). Mass spectrometry result: m/z = 177.0 [M + H]+.  |  [References]
  [1] European Journal of Organic Chemistry,  2013,  # 27,  p. 6130 - 6136 [2] Patent: US2016/376283,  2016,  A1. Location in patent: Paragraph 1225; 1226 [3] Patent: CN106187910,  2016,  A. Location in patent: Paragraph 0120; 0121 [4] European Journal of Medicinal Chemistry,  2017,  vol. 137,  p. 598 - 611 |  
  
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