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ChemicalBook--->CAS DataBase List--->37972-69-3

37972-69-3

37972-69-3 Structure

37972-69-3 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

6-Hydroxypyridazine-3-carboxylic acid is a carboxylic acid derivative and can be used as an intermediate in organic synthesis.
[Synthesis]

6-OXO-1,4,5,6-TETRAHYDROPYRIDAZIN-3-CARBOXYLIC ACID

27372-38-9

6-Oxo-1,6-dihydro-pyridazine-3-carboxylicacid

37972-69-3

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
Spectrum DetailBack Directory
[Spectrum Detail]

6-Oxo-1,6-dihydro-pyridazine-3-carboxylicacid(37972-69-3)1HNMR
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