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823-58-5

823-58-5 Structure

823-58-5 Structure
IdentificationBack Directory
[Name]

3,6-dichloropyridazin-4-amine
[CAS]

823-58-5
[Synonyms]

NSC 170664
4-Amino-3,6-dichL
3,6-dichloropyridazin-4-amine
4-Amino-3,6-dihydropyridazine
3,6-Dichloro-4-Pyridazinamine
3,6-Dichloro-4-aMinopyridazine
4-AMino-3,6-dichloropyridazine
4-AMino-3,6-dicholropyridazine
4-PyridazinaMine, 3,6-dichloro-
4-Amino-3,6-dichloropyridazine 98%
3,6-dichloropyridazin-4-amine ISO 9001:2015 REACH
3,6-Dichloropyridazin-4-amine, 4-Amino-3,6-dichloro-1,2-diazine
[Molecular Formula]

C4H3Cl2N3
[MDL Number]

MFCD01647253
[MOL File]

823-58-5.mol
[Molecular Weight]

163.99
Chemical PropertiesBack Directory
[Melting point ]

203 °C
[Boiling point ]

363.0±37.0 °C(Predicted)
[density ]

1.606±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

solid
[pka]

2.08±0.10(Predicted)
[color ]

Yellow-brown
[InChI]

InChI=1S/C4H3Cl2N3/c5-3-1-2(7)4(6)9-8-3/h1H,(H2,7,8)
[InChIKey]

HODYDVHWWMTUEL-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NN=C(Cl)C=C1N
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P280
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

3,6-dichloropyridazin-4-amine(823-58-5)1HNMR
3,6-dichloropyridazin-4-amine(823-58-5)FT-IR
Hazard InformationBack Directory
[Synthesis]

3,4,6-Trichloropyridazine

6082-66-2

3,6-dichloropyridazin-4-amine

823-58-5

General procedure for the synthesis of 3,6-dichloropyridazin-4-amine from 3,4,6-trichloropyridazine: Example 24A: 3,4,6-Trichloropyridazine (25 g, 136 mmol) was added to a 500 mL stainless steel pressure flask containing 14.8 N ammonium hydroxide solution (200 mL). The reaction mixture was stirred at 75°C for 16 hours. Upon completion of the reaction, the mixture was cooled to room temperature and the solid product was collected by filtration to afford 17 g (76% yield) of the target compound 3,6-dichloropyridazin-4-amine. The product characterization data were as follows: 1H NMR (400 MHz, DMSO-d6) δ ppm 7.16 (s, 2H), 6.82 (s, 1H); MS (ESI+) m/z 164 (M+H)+.

[References]

[1] Journal of Organic Chemistry, 2014, vol. 79, # 21, p. 10311 - 10322
[2] Patent: US2017/15675, 2017, A1. Location in patent: Paragraph 1001
[3] Patent: US2009/163489, 2009, A1. Location in patent: Page/Page column 51
[4] Patent: US2014/349990, 2014, A1. Location in patent: Paragraph 1051; 1052
[5] Patent: WO2014/191896, 2014, A1. Location in patent: Page/Page column 217; 218
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