Cas no 84487-04-7 (6-bromo-3-nitro-pyridin-2-amine)

6-bromo-3-nitro-pyridin-2-amine structure
84487-04-7 structure
Product Name:6-bromo-3-nitro-pyridin-2-amine
CAS No:84487-04-7
MF:C5H4BrN3O2
MW:218.008159637451
MDL:MFCD07774108
CID:720186
PubChem ID:12097745
Update Time:2024-10-26

6-bromo-3-nitro-pyridin-2-amine Chemical and Physical Properties

Names and Identifiers

    • 6-Bromo-3-nitropyridin-2-amine
    • 2-Pyridinamine,6-bromo-3-nitro-
    • 6-Bromo-2-bromo-3-nitropyrdine
    • 6-Bromo-3-nitro-2-pyridinamine
    • 2-Amino-6-bromo-3-nitropyridine
    • 2-amino-3-nitro-6-bromo-pyridine
    • 6-amino-2-bromo-5-nitropyridine
    • 6-bromo-3-nitro-2-pyridylamine
    • 6-bromo-3-nitro-pyridin-2-ylamine
    • 6-bromo-3-nitro-pyridin-2-amine
    • 6-Bromo-3-nitro-2-pyridinamine (ACI)
    • (6-Bromo-3-nitropyridin-2-yl)amine
    • 2-Amino-3-nitro-6-bromopyridine
    • MFCD07774108
    • SY024711
    • J-518380
    • AD-0160
    • STL556134
    • AKOS005071582
    • AC-28016
    • DB-082231
    • 84487-04-7
    • YRXZIHANXVKUHP-UHFFFAOYSA-N
    • PB20206
    • BBL102334
    • CHEMPACIFIC 38154
    • SCHEMBL1582439
    • CS-W022461
    • 2-PYRIDINAMINE, 6-BROMO-3-NITRO-
    • DTXSID00477511
    • MDL: MFCD07774108
    • Inchi: 1S/C5H4BrN3O2/c6-4-2-1-3(9(10)11)5(7)8-4/h1-2H,(H2,7,8)
    • InChI Key: YRXZIHANXVKUHP-UHFFFAOYSA-N
    • SMILES: [O-][N+](C1C(N)=NC(Br)=CC=1)=O

Computed Properties

  • Exact Mass: 216.94900
  • Monoisotopic Mass: 216.94869g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 160
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.9
  • Topological Polar Surface Area: 84.7?2

Experimental Properties

  • Density: 1.929±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 199-202°
  • Boiling Point: 349.5℃ at 760 mmHg
  • Flash Point: 165.183°C
  • Refractive Index: 1.683
  • Solubility: Slightly soluble (2.2 g/l) (25 o C),
  • PSA: 84.73000
  • LogP: 2.43890

6-bromo-3-nitro-pyridin-2-amine Security Information

  • HazardClass:IRRITANT

6-bromo-3-nitro-pyridin-2-amine Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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6-bromo-3-nitro-pyridin-2-amine Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Sulfuric acid ,  Nitric acid
2.1 Reagents: Sulfuric acid
Reference
Substituent effects on the isomer ratios in the rearrangement of some 2- and 4-nitraminopyridines
Deady, Leslie W.; et al, Australian Journal of Chemistry, 1982, 35(10), 2025-34

Production Method 2

Reaction Conditions
1.1 Reagents: Ammonia Solvents: Ethanol ;  30 min, 0 °C; 24 h, rt
Reference
Islet Amyloid-Induced Cell Death and Bilayer Integrity Loss Share a Molecular Origin Targetable with Oligopyridylamide-Based α-Helical Mimetics
Kumar, Sunil; et al, Chemistry & Biology (Oxford, 2015, 22(3), 369-378

Production Method 3

Reaction Conditions
1.1 Reagents: Hydrogen bromide Solvents: Acetic acid ;  8 h, 100 °C; 100 °C → 0 °C
1.2 Reagents: Sodium hydroxide Solvents: Water ;  pH 7, 0 °C
Reference
Carba Analogues of Flupirtine and Retigabine with Improved Oxidation Resistance and Reduced Risk of Quinoid Metabolite Formation
Wurm, Konrad W. ; et al, ChemMedChem, 2022, 17(16),

Production Method 4

Reaction Conditions
1.1 Reagents: Hydrogen bromide Solvents: Acetic acid ;  10 h, 100 °C
1.2 Reagents: Sodium bicarbonate Solvents: Water
Reference
Aminoazabenzimidazoles, a Novel Class of Orally Active Antimalarial Agents
Hameed P, Shahul; et al, Journal of Medicinal Chemistry, 2014, 57(13), 5702-5713

Production Method 5

Reaction Conditions
1.1 Reagents: Hydrogen bromide Solvents: Acetic acid
1.2 Reagents: Ammonia Solvents: Methanol
Reference
Imidazopyridine/pyrrole and hydroxybenzimidazole/pyrrole pairs for DNA minor groove recognition
Renneberg, Dorte; et al, Journal of the American Chemical Society, 2003, 125(19), 5707-5716

Production Method 6

Reaction Conditions
1.1 Reagents: Sulfuric acid
Reference
Substituent effects on the isomer ratios in the rearrangement of some 2- and 4-nitraminopyridines
Deady, Leslie W.; et al, Australian Journal of Chemistry, 1982, 35(10), 2025-34

Production Method 7

Reaction Conditions
1.1 Reagents: Hydrochloric acid
2.1 Reagents: Sulfuric acid ,  Nitric acid
3.1 Reagents: Sulfuric acid
Reference
Substituent effects on the isomer ratios in the rearrangement of some 2- and 4-nitraminopyridines
Deady, Leslie W.; et al, Australian Journal of Chemistry, 1982, 35(10), 2025-34

6-bromo-3-nitro-pyridin-2-amine Raw materials

6-bromo-3-nitro-pyridin-2-amine Preparation Products

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