ChemicalBook--->CAS DataBase List--->108784-42-5

108784-42-5

108784-42-5 Structure

108784-42-5 Structure
IdentificationBack Directory
[Name]

3-AMino-6-fluoropyridazine
[CAS]

108784-42-5
[Synonyms]

6-fluoropyridazin-3-amine
3-AMino-6-fluoropyridazine
3-Pyridazinamine, 6-fluoro-
6-Fluoro-pyridazin-3-ylaMine
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C4H4FN3
[MDL Number]

MFCD11109433
[MOL File]

108784-42-5.mol
[Molecular Weight]

113.09
Chemical PropertiesBack Directory
[storage temp. ]

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

Light yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H318-H332-H315-H335-H312-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P280-P302+P352-P312-P322-P363-P501-P264-P280-P302+P352-P321-P332+P313-P362-P280-P305+P351+P338-P310
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

3-AMino-6-fluoropyridazine(108784-42-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

3,6-difluoropyridazine

33097-39-1

3-AMino-6-fluoropyridazine

108784-42-5

The general procedure for the synthesis of 6-fluoropyridazin-3-amine from 3,6-difluoropyridazine was as follows: 3,6-difluoropyridazine (60.3 mmol) was mixed with 25 mL of ammonia in a sealed reaction tube and reacted at 70 °C for 2 hours. After completion of the reaction, it was cooled to room temperature and the precipitate was collected by filtration. Subsequently, the precipitate was washed with water and dried to give 6-fluoropyridazin-3-amine in a yield of 4.28 g. The reaction was carried out in a sealed reaction tube.

[References]

[1] Australian Journal of Chemistry, 1986, vol. 39, # 11, p. 1803 - 1809
[2] Patent: US5049558, 1991, A
[3] ACS Medicinal Chemistry Letters, 2010, vol. 1, # 2, p. 80 - 84
[4] Patent: CN103130792, 2016, B. Location in patent: Paragraph 0582-0584
[5] Patent: CN103130791, 2016, B. Location in patent: Paragraph 0406-0408
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