ChemicalBook--->CAS DataBase List--->17321-20-9

17321-20-9

17321-20-9 Structure

17321-20-9 Structure
IdentificationBack Directory
[Name]

3-CHLORO-6-ETHOXYPYRIDAZINE
[CAS]

17321-20-9
[Synonyms]

NSC 94042
3-CHLORO-6-ETHOXYPYRIDAZINE
Pyridazine, 3-chloro-6-ethoxy-
3-chloro-6-ethoxypyridazine(SALTDATA: FREE)
3-CHLORO-6-ETHOXYPYRIDAZINE ISO 9001:2015 REACH
[Molecular Formula]

C6H7ClN2O
[MDL Number]

MFCD00270290
[MOL File]

17321-20-9.mol
[Molecular Weight]

158.59
Chemical PropertiesBack Directory
[Melting point ]

60-62℃
[Boiling point ]

293.1±20.0 °C(Predicted)
[density ]

1.235
[storage temp. ]

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

0.82±0.10(Predicted)
[Appearance]

Off-white to yellow 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
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

3-CHLORO-6-ETHOXYPYRIDAZINE(17321-20-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

3,6-Dichloropyridazine

141-30-0

Ethanol

64-17-5

3-CHLORO-6-ETHOXYPYRIDAZINE

17321-20-9

Potassium carbonate (1.39 g, 10.05 mmol) was added to a 50 mL round-bottomed flask containing 3,6-dichloropyridazine (1.00 g, 6.71 mmol) and anhydrous ethanol (10 mL). The reaction mixture was stirred under ethanol reflux for 22 hours. After completion of the reaction, it was cooled to room temperature, saturated ammonium chloride solution (30 mL) was added and the reaction mixture was extracted with dichloromethane (3 x 30 mL). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was ground with petroleum ether and filtered through a Büchner funnel to give the pure 3-chloro-6-ethoxypyridazine (1.025 g, 97% yield).

[References]

[1] Tetrahedron, 2015, vol. 71, # 29, p. 4859 - 4867
[2] Yakugaku Zasshi, 1954, vol. 74, p. 1195,1197
[3] Chem.Abstr., 1955, p. 14768
[4] Yakugaku Zasshi, 1955, vol. 75, p. 778,780
[5] Chem.Abstr., 1956, p. 4970
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