ChemicalBook--->CAS DataBase List--->6641-32-3

6641-32-3

6641-32-3 Structure

6641-32-3 Structure
IdentificationBack Directory
[Name]

4,5-DICHLORO-3,6-PYRIDAZINEDIOL
[CAS]

6641-32-3
[Synonyms]

4,5-DICHLOROPYRIDAZINE-3,6-DIOL
4,5-DICHLORO-3,6-PYRIDAZINEDIOL
4,5-Dichlor-3,6-dihydroxy-pyridazin
3(2H)-Pyridazinone, 4,5-dichloro-6-hydroxy-
4,5-dichloro-1,2-dihydropyridazine-3,6-dione
[Molecular Formula]

C4H2Cl2N2O2
[MDL Number]

MFCD00834958
[MOL File]

6641-32-3.mol
[Molecular Weight]

180.98
Chemical PropertiesBack Directory
[Melting point ]

295
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

4,5-DICHLORO-3,6-PYRIDAZINEDIOL(6641-32-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

Dichloromaleic anhydride

1122-17-4

4,5-DICHLORO-3,6-PYRIDAZINEDIOL

6641-32-3

General procedure for the synthesis of 4,5-dichloropyridazine-3,6-diol from 2,3-dichloromaleic anhydride: water (170 mL) and hydrazine dihydrochloride salt (41.9 g, 398.8 mmol) were added to a round bottom flask. The solution was heated to reflux followed by the addition of 2,3-dichloromaleic anhydride (66.6 g, 398.9 mmol) in batches. The reflux condition was maintained and the reaction mixture was stirred continuously for 30 minutes. Upon completion of the reaction, the solution was cooled to room temperature and the precipitated solid was collected by filtration to afford the target product 4,5-dichloropyridazine-3,6-diol (i.e., 4,5-dichloro-1,2-dihydropyridazine-3,6-dione, 65 g, 90% yield) as a white solid. Mass spectral analysis showed (M + H)+ = 181.0.

[References]

[1] Patent: US2006/287323, 2006, A1. Location in patent: Page/Page column 7
[2] Zhurnal Obshchei Khimii, 1954, vol. 24, p. 1216,1219; engl. Ausg. S. 1205, 1206
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