Cas no 2423-74-7 (Phenol, 2,6-dibromo-4-methoxy-)

Phenol, 2,6-dibromo-4-methoxy-, is a brominated phenolic compound characterized by its distinct substitution pattern, featuring methoxy and bromo functional groups at the 4- and 2,6-positions, respectively. This structural configuration enhances its stability and reactivity, making it a valuable intermediate in organic synthesis, particularly for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The electron-withdrawing bromo groups and electron-donating methoxy group contribute to its unique electronic properties, facilitating selective transformations in cross-coupling and electrophilic substitution reactions. Its high purity and well-defined structure ensure consistent performance in demanding applications. Proper handling is advised due to its potential reactivity and halogenated nature.
Phenol, 2,6-dibromo-4-methoxy- structure
2423-74-7 structure
Product Name:Phenol, 2,6-dibromo-4-methoxy-
CAS No:2423-74-7
MF:C7H6Br2O2
MW:281.929340839386
MDL:MFCD12755175
CID:1416656
PubChem ID:13723714
Update Time:2025-05-22

Phenol, 2,6-dibromo-4-methoxy- Chemical and Physical Properties

Names and Identifiers

    • Phenol, 2,6-dibromo-4-methoxy-
    • 2,6-dibromo-4-methoxyphenol
    • F15247
    • 2423-74-7
    • 2,6-dibromo-4-methoxy-phenol
    • SCHEMBL1119249
    • AKOS030529280
    • AML0050
    • MFCD12755175
    • DTXSID70547674
    • NS-00121
    • SGIZMXOUTHAIAN-UHFFFAOYSA-N
    • NS00133703
    • MDL： MFCD12755175
    • Inchi： 1S/C7H6Br2O2/c1-11-4-2-5(8)7(10)6(9)3-4/h2-3,10H,1H3
    • InChI Key： SGIZMXOUTHAIAN-UHFFFAOYSA-N
    • SMILES： BrC1C(=C(C=C(C=1)OC)Br)O

Computed Properties

  • Exact Mass: 279.87338
  • Monoisotopic Mass: 279.87345g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 120
  • 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: 3.7
  • Topological Polar Surface Area: 29.5?2

Experimental Properties

  • PSA: 29.46

Phenol, 2,6-dibromo-4-methoxy- Pricemore >>

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Phenol, 2,6-dibromo-4-methoxy- Related Literature

Additional information on Phenol, 2,6-dibromo-4-methoxy-

Comprehensive Analysis of Phenol, 2,6-dibromo-4-methoxy- (CAS No. 2423-74-7)

Phenol, 2,6-dibromo-4-methoxy- (CAS No. 2423-74-7) is a halogenated phenolic compound with significant applications in organic synthesis and material science. This compound, also known as 2,6-dibromo-4-methoxyphenol, features a methoxy group and two bromine atoms attached to a phenolic ring, which enhances its reactivity and utility in various chemical processes. Researchers and industries value this compound for its unique properties, including its role as an intermediate in the synthesis of more complex molecules.

The growing interest in halogenated phenols like Phenol, 2,6-dibromo-4-methoxy- is driven by their versatility in pharmaceuticals, agrochemicals, and specialty chemicals. With increasing demand for sustainable and efficient synthetic routes, this compound has gained attention for its potential in green chemistry applications. Users often search for "2,6-dibromo-4-methoxyphenol uses" or "CAS 2423-74-7 synthesis," reflecting the need for detailed technical insights.

From a structural perspective, the presence of bromine atoms in Phenol, 2,6-dibromo-4-methoxy- makes it a valuable building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are pivotal in modern organic chemistry. The methoxy group further modifies its electronic properties, enabling selective functionalization. These characteristics align with current trends in "highly functionalized aromatic compounds" and "brominated intermediates," which are frequently explored in academic and industrial research.

Environmental and safety considerations are also critical when discussing Phenol, 2,6-dibromo-4-methoxy-. While it is not classified as hazardous under standard regulations, proper handling and disposal protocols are essential to minimize ecological impact. Searches like "2,6-dibromo-4-methoxyphenol safety data" highlight user concerns about responsible usage, reflecting broader societal emphasis on chemical sustainability.

In analytical chemistry, CAS No. 2423-74-7 is often characterized using techniques such as NMR, HPLC, and mass spectrometry. These methods ensure purity and confirm structural integrity, addressing common queries like "how to analyze 2,6-dibromo-4-methoxyphenol." The compound's distinct spectral signatures make it a useful reference in method development and quality control.

Looking ahead, the applications of Phenol, 2,6-dibromo-4-methoxy- are expected to expand, particularly in advanced materials and bioactive molecule synthesis. Its compatibility with emerging technologies, such as flow chemistry and catalytic systems, positions it as a compound of interest for future innovations. By addressing user-driven questions like "2423-74-7 in drug discovery" or "brominated phenol derivatives," this overview bridges technical expertise with practical relevance.

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