Cas no 26163-05-3 (3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine)

3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine is a halogenated nitropyridine derivative with a dimethylamino substituent, serving as a versatile intermediate in organic synthesis and pharmaceutical research. Its bromo and nitro functional groups enhance reactivity, enabling selective cross-coupling reactions and nucleophilic substitutions. The electron-withdrawing nitro group and electron-donating dimethylamino moiety create a polarized structure, facilitating applications in heterocyclic chemistry. This compound is particularly valuable in the development of agrochemicals, pharmacophores, and materials science due to its stable yet modifiable framework. High purity grades ensure consistent performance in synthetic pathways, making it a reliable choice for researchers requiring precise functionalization of pyridine-based scaffolds.
3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine structure
26163-05-3 structure
Product Name:3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine
CAS No:26163-05-3
MF:C7H8BrN3O2
MW:246.061320304871
CID:852224
PubChem ID:3760936
Update Time:2025-06-13

3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine Chemical and Physical Properties

Names and Identifiers

    • 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine
    • 3-Bromo-2-(N,N-dimethyl)amino-5-nitropyridine
    • (3-bromo-5-nitro-pyridin-2-yl)-dimethyl-amine
    • 3-Brom-2-dimethylamino-5-nitropyridin
    • MFCD00955983
    • 26163-05-3
    • 2-Pyridinamine, 3-bromo-N,N-dimethyl-5-nitro-
    • AKOS015834048
    • DTXSID60396052
    • BS-22145
    • BBA16305
    • CS-0211949
    • MDL: MFCD00955983
    • Inchi: 1S/C7H8BrN3O2/c1-10(2)7-6(8)3-5(4-9-7)11(12)13/h3-4H,1-2H3
    • InChI Key: MPBCWXXDYWCJSW-UHFFFAOYSA-N
    • SMILES: BrC1=CC(=CN=C1N(C)C)[N+](=O)[O-]

Computed Properties

  • Exact Mass: 244.98000
  • Monoisotopic Mass: 244.97999g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 195
  • 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: 1.8
  • Topological Polar Surface Area: 62?2

Experimental Properties

  • Density: 1.7±0.1 g/cm3
  • Melting Point: 45-48℃
  • Boiling Point: 319.4±42.0 °C at 760 mmHg
  • Flash Point: 146.9±27.9 °C
  • PSA: 61.95000
  • LogP: 2.34150
  • Vapor Pressure: 0.0±0.7 mmHg at 25°C

3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine Security Information

3-Bromo-N,N-dimethyl-5-nitropyridin-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%

3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine Pricemore >>

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Additional information on 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine

Recent Advances in the Study of 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine (CAS: 26163-05-3)

The compound 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine (CAS: 26163-05-3) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This heterocyclic compound, characterized by its bromo and nitro functional groups, has shown promising potential in various applications, including drug discovery and material science. Recent studies have focused on its synthesis, reactivity, and biological activity, providing new insights into its utility as a building block for more complex molecules.

One of the key areas of research involves the optimization of synthetic routes for 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine. A study published in the Journal of Organic Chemistry (2023) demonstrated an efficient, high-yield synthesis method using palladium-catalyzed cross-coupling reactions. This advancement not only improves the accessibility of the compound but also reduces the environmental impact of its production, aligning with the growing emphasis on green chemistry in pharmaceutical manufacturing.

In addition to its synthetic applications, 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine has been investigated for its biological activity. Preliminary in vitro studies have revealed its potential as an inhibitor of certain kinase enzymes, which are often implicated in cancer and inflammatory diseases. A recent paper in Bioorganic & Medicinal Chemistry Letters (2024) highlighted its moderate inhibitory activity against EGFR (Epidermal Growth Factor Receptor), suggesting its potential as a lead compound for the development of novel anticancer agents.

Further research has explored the compound's role in material science. Due to its unique electronic properties, 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine has been incorporated into organic semiconductors and photovoltaic materials. A study in Advanced Materials (2023) reported its use in the fabrication of organic light-emitting diodes (OLEDs), where it contributed to improved device efficiency and stability. These findings underscore the versatility of this compound beyond traditional pharmaceutical applications.

Despite these promising developments, challenges remain in the full characterization and application of 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine. Issues such as its stability under physiological conditions and potential toxicity profiles require further investigation. Ongoing research aims to address these gaps, with several collaborative projects between academia and industry currently underway. The compound's future in drug discovery and material science appears bright, provided these challenges can be effectively mitigated.

In conclusion, 3-Bromo-N,N-dimethyl-5-nitropyridin-2-amine (CAS: 26163-05-3) represents a valuable scaffold in both pharmaceutical and material science research. Recent advancements in its synthesis and application highlight its potential, while also pointing to areas where further study is needed. As research continues, this compound is likely to play an increasingly important role in the development of new therapeutic agents and advanced materials.

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