Cas no 853953-36-3 (Benzenamine, 2,4-dibromo-3-methoxy-)

Benzenamine, 2,4-dibromo-3-methoxy- structure
853953-36-3 structure
Product Name:Benzenamine, 2,4-dibromo-3-methoxy-
CAS No:853953-36-3
MF:C7H7Br2NO
MW:280.944580316544
CID:1837362
PubChem ID:14952459
Update Time:2025-09-23

Benzenamine, 2,4-dibromo-3-methoxy- Chemical and Physical Properties

Names and Identifiers

    • Benzenamine, 2,4-dibromo-3-methoxy-
    • 2,4-DIBROMO-3-METHOXYANILINE
    • 853953-36-3
    • Inchi: 1S/C7H7Br2NO/c1-11-7-4(8)2-3-5(10)6(7)9/h2-3H,10H2,1H3
    • InChI Key: OFWIOFYEZQQRGJ-UHFFFAOYSA-N
    • SMILES: BrC1C(=CC=C(C=1OC)Br)N

Computed Properties

  • Exact Mass: 280.88739g/mol
  • Monoisotopic Mass: 278.88944g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 134
  • 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: 2.6
  • Topological Polar Surface Area: 35.2?2

Benzenamine, 2,4-dibromo-3-methoxy- Pricemore >>

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Additional information on Benzenamine, 2,4-dibromo-3-methoxy-

Comprehensive Analysis of Benzenamine, 2,4-dibromo-3-methoxy- (CAS No. 853953-36-3): Properties, Applications, and Industry Trends

Benzenamine, 2,4-dibromo-3-methoxy- (CAS No. 853953-36-3) is a halogenated aniline derivative with significant relevance in organic synthesis and specialty chemical industries. This compound, characterized by its bromine and methoxy functional groups, exhibits unique reactivity patterns that make it valuable for constructing complex molecular architectures. As demand for fine chemicals and pharmaceutical intermediates grows, researchers are increasingly exploring the potential of this brominated aniline derivative.

The structural features of 2,4-dibromo-3-methoxyaniline contribute to its versatility. The electron-withdrawing bromine atoms at the 2- and 4-positions, combined with the electron-donating methoxy group at the 3-position, create an interesting electronic environment that influences its reactivity in cross-coupling reactions and nucleophilic substitutions. These properties align with current industry trends toward atom-efficient synthesis and green chemistry principles.

Recent advancements in catalyzed reactions have highlighted the utility of 853953-36-3 as a building block. Its applications span from agrochemical intermediates to dye precursors, with particular interest in its potential for creating liquid crystal materials. The compound's stability under various conditions makes it suitable for multistep synthesis workflows, addressing the growing need for modular chemical platforms in research and development.

From a safety and handling perspective, proper laboratory protocols should always be followed when working with halogenated compounds. While not classified as hazardous under normal conditions, standard precautions for organic synthesis apply. The compound's physicochemical properties, including its melting point and solubility characteristics, have been well-documented to facilitate its use in various chemical processes.

The synthesis and applications of Benzenamine, 2,4-dibromo-3-methoxy- continue to evolve alongside developments in sustainable chemistry. Researchers are investigating its potential in catalyzed transformations and as a precursor for functional materials. As the chemical industry shifts toward more specialty applications, compounds like 853953-36-3 are gaining attention for their structural versatility and synthetic utility.

Quality control measures for 2,4-dibromo-3-methoxyaniline typically involve advanced analytical techniques such as HPLC and NMR spectroscopy. These methods ensure the compound meets the purity standards required for pharmaceutical-grade intermediates and other high-value applications. The growing emphasis on process optimization in chemical manufacturing has led to improved synthetic routes for this brominated aromatic amine.

Market trends indicate increasing demand for halogenated building blocks like 853953-36-3, particularly in regions with strong pharmaceutical innovation ecosystems. The compound's role in developing new chemical entities aligns with current research priorities in medicinal chemistry and material science. As synthetic methodologies advance, we can expect to see expanded applications for this versatile chemical intermediate.

Environmental considerations surrounding brominated compounds have prompted research into improved waste management strategies and degradation pathways. While Benzenamine, 2,4-dibromo-3-methoxy- doesn't present significant environmental concerns when handled properly, the industry continues to develop better handling protocols and disposal methods for all specialty chemicals.

Looking ahead, the scientific community anticipates new discoveries involving 853953-36-3 as researchers explore its potential in asymmetric synthesis and cascade reactions. The compound's unique substitution pattern offers opportunities for creating chiral auxiliaries and ligand systems, areas of significant interest in contemporary organic chemistry research.

For laboratories and manufacturers working with 2,4-dibromo-3-methoxyaniline, proper storage conditions and handling procedures remain essential considerations. The compound's stability under various conditions has been well-characterized, supporting its use in diverse chemical applications. As with all research chemicals, users should consult updated safety data and technical specifications before beginning any experimental work.

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