Cas no 55814-63-6 (5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene)

5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene is a halogenated aromatic compound featuring bromo, chloro, and methoxyphenoxy substituents, offering versatile reactivity for synthetic applications. Its distinct substitution pattern enables selective functionalization, making it valuable in pharmaceutical and agrochemical intermediate synthesis. The electron-rich methoxyphenoxy group enhances stability while facilitating further derivatization. The bromo and chloro groups provide reactive sites for cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, broadening its utility in complex molecule construction. This compound’s well-defined structure and functional group compatibility make it a reliable building block for researchers developing advanced organic frameworks. Its high purity and consistent performance ensure reproducibility in demanding synthetic workflows.
5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene structure
55814-63-6 structure
Product Name:5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene
CAS No:55814-63-6
MF:C13H9BrCl2O2
MW:348.019361257553
CID:1027997
PubChem ID:70700441
Update Time:2025-08-05

5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene Chemical and Physical Properties

Names and Identifiers

    • 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene
    • Benzene, 5-bromo-1,3-dichloro-2-(4-methoxyphenoxy)-
    • LogP
    • 55814-63-6
    • SCHEMBL23663156
    • DTXSID50743273
    • DB-072052
    • MDL: MFCD14706740
    • Inchi: 1S/C13H9BrCl2O2/c1-17-9-2-4-10(5-3-9)18-13-11(15)6-8(14)7-12(13)16/h2-7H,1H3
    • InChI Key: KGHTYPVKRDRRBL-UHFFFAOYSA-N
    • SMILES: BrC1C=C(C(=C(C=1)Cl)OC1C=CC(=CC=1)OC)Cl

Computed Properties

  • Exact Mass: 345.91637
  • Monoisotopic Mass: 345.91630g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 3
  • Complexity: 247
  • 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: 4.9
  • Topological Polar Surface Area: 18.5?2

Experimental Properties

  • Density: 1.553
  • Boiling Point: 359.348°C at 760 mmHg
  • Flash Point: 171.128°C
  • Refractive Index: 1.602
  • PSA: 18.46

5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene Pricemore >>

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Additional information on 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene

5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene: A Comprehensive Overview

5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene (CAS No. 55814-63-6) is a complex organic compound with a diverse range of applications in various industries. This compound, often referred to as Bromo-Dichloro-Phenoxybenzene, has garnered significant attention due to its unique chemical properties and potential uses in pharmaceuticals, agrochemicals, and advanced materials. Recent studies have highlighted its role in enhancing the efficiency of certain chemical processes, making it a subject of interest for researchers and industry professionals alike.

The structure of 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene is characterized by a benzene ring with substituents at specific positions. The bromine atom at position 5, chlorine atoms at positions 1 and 3, and the phenoxy group at position 2 create a highly functionalized molecule. This functionalization not only contributes to its stability but also enables it to participate in various chemical reactions, such as nucleophilic aromatic substitution and electrophilic substitution. Recent research has explored the use of this compound as an intermediate in the synthesis of bioactive molecules, particularly in the development of novel antibiotics and antiviral agents.

One of the most notable advancements involving Bromo-Dichloro-Phenoxybenzene is its application in the field of polymer chemistry. Scientists have discovered that this compound can serve as a building block for the creation of high-performance polymers with improved thermal stability and mechanical properties. These polymers have potential applications in aerospace, automotive industries, and electronic devices where durability under extreme conditions is paramount.

In addition to its industrial applications, 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene has also been studied for its environmental impact. Researchers have investigated its biodegradation pathways and toxicity levels to aquatic organisms. Findings suggest that while the compound exhibits moderate toxicity, it can be effectively treated through advanced wastewater treatment processes, minimizing its ecological footprint.

The synthesis of Bromo-Dichloro-Phenoxybenzene involves a multi-step process that requires precise control over reaction conditions to ensure high yield and purity. Recent innovations in catalytic chemistry have enabled more efficient synthesis methods, reducing production costs and environmental impact. These advancements have made the compound more accessible for large-scale industrial use.

Looking ahead, the future of 5-Bromo-1,3-dichloro-2-(4-methoxyphenoxy)benzene seems promising as researchers continue to uncover new applications and improve existing ones. Its role in drug discovery, polymer development, and environmental remediation underscores its versatility and importance in modern chemistry.

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