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Home > Encyclopedia > 4,6-dibromopyridazin-3-amine

4,6-dibromopyridazin-3-amine

4,6-dibromopyridazin-3-amine structure

4,6-dibromopyridazin-3-amine 

structure
  • CAS No:

    1206487-35-5

  • Formula:

    C4H3Br2N3

  • Chemical Name:

    4,6-dibromopyridazin-3-amine

  • Synonyms:

    4,6-DIBROMOPYRIDAZIN-3-AMINE;4,6-dibromo-3-Pyridazinamine;ACMC-20aco7;3-amino-4,6-dibromopyridazine;SCHEMBL1576635;CTK4B1956;DTXSID40673176;KS-000000DJ;3573AA;ANW-67349

4,6-dibromopyridazin-3-amine Basic Attributes

253

250.86900

DTXSID40673176

2933990090

Characteristics

51.8

1.2

2.287±0.06 g/cm3(Predicted)

376.6±37.0 °C(Predicted)

4,6-dibromopyridazin-3-amine Use and Manufacturing

To a mixture comprising 285 g (1638 mmol) 6-bromopyridazin-3-amine which was prepared according to intermediate example 30h, 275 g (3276 mmol) NaHCCb and 2815 mL MeOH was dropwise added 85 mL (1638 mmol) bromine at rt and it was stirred at rt overnight. After further addition of 34 mL (655 mmol) bromine and 55 g (655 mmol) NaHC03, the mixture was stirred overnight again. The solvent was reduced to about 1000 mL and the mixture was poured on 5 L of water. The precipitate was filtered off, washed with water and dried give 41 1 g (99percent) of the title compound. 1 H-NMR (CDCla): δ= 6.14 (1 H), 9.92 (2H) ppm.To a mixture comprising 285 g (1638 mmol) 6-bromopyridazin-3-amine which was prepared according to intermediate h, 275 g (3276 mmol) NaHC03 and 2815 mL MeOH was dropwise added 85 mL (1638 mmol) bromine at rt and it was stirred at rt overnight. After further addition of 34 mL (655 mmol) bromine and 55 g (655 mmol) NaHC03, the mixture was stirred overnight again. The solvent was reduced to about 1000 mL and the mixture was poured on 5 L of water. The precipitate was filtered off, washed with water and dried give 411 g (99percent) of the title compound. Intermediate Example 26 6, 8-dibromoimidazo[1 , 2-b]pyridazine To a mixture comprising 285 g (1638 mmol) 6-bromopyridazin-3-amine which was prepared according to intermediate example 26h, 275 g (3276 mmol) NaHC03 and 2815 mL MeOH was dropwise added 85 mL (1638 mmol) bromine at rt and it was stirred at rt overnight. After further addition of 34 mL (655 mmol) bromine and 55 g (655 mmol) NaHC03, the mixture was stirred overnight again. The solvent was reduced to about 1000 mL and the mixture was poured on 5 L of water. The precipitate was filtered off, washed with water and dried give 411 g (99percent) of the title compound. 1 H-NMR (CDCb): δ= 6.14 (1 H), 9.92 (2H) ppm.

Computed Properties

Molecular Weight:252.89
XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Exact Mass:252.86732
Monoisotopic Mass:250.86937
Topological Polar Surface Area:51.8
Heavy Atom Count:9
Complexity:99.8
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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