ChemicalBook--->CAS DataBase List--->15456-86-7

15456-86-7

15456-86-7 Structure

15456-86-7 Structure
IdentificationBack Directory
[Name]

Pyridazine, 3,6-dione, 4-bromo-1,2-dihydro-
[CAS]

15456-86-7
[Synonyms]

Nsc79701
4-Bromopyridazine-3,6-diol
4-Bromo-3-hydroxy-6-pyridazinone
4-Bromo-6-Hydroxy-3(2H)-Pyridazinone
3(2H)-Pyridazinone, 4-bromo-6-hydroxy-
4-Bromo-1,2-dihydropyridazine-3,6-dione
Pyridazine, 3,6-dione, 4-bromo-1,2-dihydro-
Pyridazine, 3,6-dione, 4-bromo-1,2-dihydro- ISO 9001:2015 REACH
[EINECS(EC#)]

200-001-2
[Molecular Formula]

C4H3BrN2O2
[MDL Number]

MFCD12923098
[MOL File]

15456-86-7.mol
[Molecular Weight]

190.99
Chemical PropertiesBack Directory
[density ]

1.965±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

7?+-.0.40(Predicted)
[Appearance]

White to off-white Solid
Questions And AnswerBack Directory
[Application]

4-Bromo-3,6-pyridazindione is a ketone organic compound that can be used as an organic reagent.
Spectrum DetailBack Directory
[Spectrum Detail]

Pyridazine, 3,6-dione, 4-bromo-1,2-dihydro-(15456-86-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

BROMOMALEIC ANHYDRIDE

5926-51-2

Pyridazine, 3,6-dione, 4-bromo-1,2-dihydro-

15456-86-7

The general procedure for the synthesis of 4-bromo-3,6-pyridazinedione from bromomaleic anhydride was as follows: hydrazine sulfate (2.25 g, 17.2 mmol) was dissolved in boiling water (20 mL) under stirring conditions. Bromomaleic anhydride (2.6 mL, 28.2 mmol) was added dropwise to this solution through an addition funnel. The reaction mixture was heated under reflux conditions (100 °C) for 19 h and subsequently cooled to room temperature. The reaction mixture was filtered through a medium glass material sintered glass funnel and a white precipitate was collected. The precipitate was washed with acetone (3 x 5 mL) and then dried under vacuum to afford the target product 4-bromo-1,2-dihydropyridazine-3,6-dione (2.85 g) as a white powder in 87% yield (based on gravimetric analysis) with a melting point of 262°C.

[References]

[1] Journal of Organic Chemistry, 2014, vol. 79, # 21, p. 10311 - 10322
[2] Patent: WO2014/145485, 2014, A2. Location in patent: Paragraph 00207; 00290
[3] Tetrahedron Letters, 2017, vol. 58, # 14, p. 1373 - 1375
[4] Patent: US6579875, 2003, B1
[5] Patent: US6303605, 2001, B1
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