ChemicalBook--->CAS DataBase List--->1632-74-2

1632-74-2

1632-74-2 Structure

1632-74-2 Structure
IdentificationBack Directory
[Name]

3,6-Dimethyl Pyridazine
[CAS]

1632-74-2
[Synonyms]

3,6-dimethylpyridazin
3,6-Dimethyl Pyridazine
Pyridazine, 3,6-diMethyl-
3,6-Dimethyl Pyridazine ISO 9001:2015 REACH
[Molecular Formula]

C6H8N2
[MDL Number]

MFCD06637608
[MOL File]

1632-74-2.mol
[Molecular Weight]

108.14
Chemical PropertiesBack Directory
[Melting point ]

32-33℃
[Boiling point ]

228℃
[density ]

0.997
[Fp ]

100℃
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

4.04±0.10(Predicted)
[Appearance]

Light yellow to yellow <32°C Solid,>33°C Liquid
[InChI]

InChI=1S/C6H8N2/c1-5-3-4-6(2)8-7-5/h3-4H,1-2H3
[InChIKey]

BGVTUIRPHLSMJU-UHFFFAOYSA-N
[SMILES]

C1(C)=NN=C(C)C=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

3,6-Dimethyl Pyridazine(1632-74-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,5-Hexanedione

110-13-4

3,6-Dimethyl Pyridazine

1632-74-2

Step A: A mixed solution of 2,5-hexanedione (6 mL, 51 mmol) and hydrazine monohydrate (2.5 mL, 51 mmol) in ethanol (50 mL) was heated to reflux for 3 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure. The residue was mixed with 10% Pd/C catalyst (1.1 g) in anhydrous benzene (200 mL) and heated to reflux overnight. After the reaction mixture was cooled to room temperature, it was filtered through a diatomaceous earth pad to remove the catalyst. The filtrate was concentrated and purified by silica gel column chromatography (eluent: dichloromethane solution containing 6% methanol) to afford 3,6-dimethylpyrazine (3.1 g, 56% yield) as a light brown oil.1H NMR (500 MHz, CDCl3): δ 7.23 (2H, s), 2.69 (6H, s).

[References]

[1] Patent: US9617268, 2017, B2. Location in patent: Page/Page column 395; 396
[2] Journal of the American Chemical Society, 1956, vol. 78, p. 1961,1964
[3] Journal of the American Chemical Society, 1938, vol. 60, p. 2456
[4] Journal of the Chemical Society - Dalton Transactions, 1996, # 10, p. 2117 - 2122
[5] Gazzetta Chimica Italiana, 1950, vol. 80, p. 783,786
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