| Identification | Back Directory | [Name]
6-oxo-1,6-dihydropyridazine-4-carboxylicacid | [CAS]
867130-58-3 | [Synonyms]
5-Carboxypyridazin-3(2H)-one
6-oxo-1H-pyridazine-4-carboxylic acid
1,6-Dihydro-6-oxo-pyridazin-4-carboxylic acid
3-oxo-2,3-dihydropyridazine-5-carboxylic acid
1,6-dihydro-6-oxo-4-pyridazinecarboxylic acid
1,6-Dihydro-6-oxopyridazine-4-carboxylic acid
4-Pyridazinecarboxylic acid, 1,6-dihydro-6-oxo-
1,6-Dihydro-6-oxopyridazine-4-carboxylic acid 95+%
6-oxo-1,6-dihydropyridazine-4-carboxylicacid ISO 9001：2015 REACH | [Molecular Formula]
C5H4N2O3 | [MDL Number]
MFCD08437486 | [MOL File]
867130-58-3.mol | [Molecular Weight]
140.1 |
| Chemical Properties | Back Directory | [Melting point ]
303 °C | [density ]
1.63±0.1 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
solid | [pka]
1.86±0.20(Predicted) | [Appearance]
Light brown to dark brown Solid | [InChI]
InChI=1S/C5H4N2O3/c8-4-1-3(5(9)10)2-6-7-4/h1-2H,(H,7,8)(H,9,10) | [InChIKey]
PSMIHCDKMNXTAY-UHFFFAOYSA-N | [SMILES]
C1=NNC(=O)C=C1C(O)=O |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 6-keto-1,6-dihydropyridazine-4-carboxylic acid from 5-methyl-3(2H)-pyridazinone: 5-methyl-3(2H)-pyridazinone (0.90 g, 8.2 mmol) was dissolved in concentrated sulfuric acid (13 mL), stirred and heated to 45 °C. Potassium permanganate (3.6 g, 12 mmol) was added in batches over a period of 30 min to control the reaction temperature to avoid a dramatic increase. After addition, the reaction was continued at 45°C with stirring for 30 minutes. After completion of the reaction, it was cooled to room temperature and quenched by adding ice water to the reaction mixture. The precipitate precipitated was collected by vacuum filtration and washed sequentially with cold water and ether to afford 0.98 g (87% yield) of the target product 6-keto-1,6-dihydropyridazine-4-carboxylic acid as a light green solid. The product was characterized by 1H NMR (300 MHz, CDCl3): δ 13.39 (broad single peak, 1H), 8.12 (single peak, 1H), 7.22 (single peak, 1H). | [References]
[1] Patent: US2007/259860, 2007, A1. Location in patent: Page/Page column 31-32
[2] Patent: WO2008/41075, 2008, A1. Location in patent: Page/Page column 55
[3] Patent: WO2008/41075, 2008, A1. Location in patent: Page/Page column 55
[4] Patent: US2007/259862, 2007, A1. Location in patent: Page/Page column 30
[5] Patent: US2009/111820, 2009, A1. Location in patent: Page/Page column 22 |
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