Cas no 1261919-61-2 (4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol)

4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol is a fluorinated phenolic compound with potential applications in pharmaceutical and chemical research due to its unique structural properties. The presence of both hydroxyl and methoxy groups on the aromatic ring, along with a fluorine substituent, enhances its reactivity and selectivity in synthetic pathways. This compound may serve as a key intermediate in the development of bioactive molecules, including drug candidates or specialty chemicals. Its well-defined molecular structure allows for precise modifications, making it valuable for studies in medicinal chemistry and material science. High purity and stability further contribute to its utility in advanced research applications.
4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol structure
1261919-61-2 structure
Product Name:4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol
CAS No:1261919-61-2
MF:C13H11FO3
MW:234.223047494888
MDL:MFCD18315053
CID:2763471
PubChem ID:53220795
Update Time:2025-11-01

4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol Chemical and Physical Properties

Names and Identifiers

    • 4-(4-FLUORO-2-HYDROXYPHENYL)-2-METHOXYPHENOL
    • MFCD18315053
    • 1261919-61-2
    • 4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol, 95%
    • DTXSID30685501
    • 4-Fluoro-3'-methoxy[1,1'-biphenyl]-2,4'-diol
    • 4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol
    • MDL： MFCD18315053
    • Inchi： 1S/C13H11FO3/c1-17-13-6-8(2-5-11(13)15)10-4-3-9(14)7-12(10)16/h2-7,15-16H,1H3
    • InChI Key： CALPJJSCWNOFMK-UHFFFAOYSA-N
    • SMILES： FC1C=CC(=C(C=1)O)C1C=CC(=C(C=1)OC)O

Computed Properties

  • Exact Mass: 234.06922237Da
  • Monoisotopic Mass: 234.06922237Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 2
  • Complexity: 249
  • 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: 2.9
  • Topological Polar Surface Area: 49.7?2

4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB321232-5 g
4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol, 95%; .
 1261919-61-2 95%
5g
 €1159.00 2023-04-26
abcr
AB321232-5g
4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol, 95%; .
 1261919-61-2 95%
5g
 €1159.00 2025-03-19

4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol Related Literature

Additional information on 4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol

4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol (CAS No. 1261919-61-2)

4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol, also known by its CAS registry number CAS No. 1261919-61-2, is a structurally complex aromatic compound with significant potential in various chemical and pharmaceutical applications. This compound, characterized by its unique substitution pattern on the phenolic ring, has garnered attention in recent years due to its versatile properties and promising research outcomes.

The molecular structure of 4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol comprises a central phenol ring substituted with a fluorine atom at the para position, a hydroxyl group at the ortho position, and a methoxy group at the meta position. This arrangement imparts distinctive electronic and steric effects, making it a valuable substrate for further chemical modifications. Recent studies have highlighted its role as an intermediate in the synthesis of advanced materials and bioactive compounds.

One of the most notable advancements involving this compound is its application in drug discovery. Researchers have explored its potential as a lead molecule for developing novel anti-inflammatory and antioxidant agents. The presence of hydroxyl and methoxy groups facilitates hydrogen bonding, which is crucial for bioavailability and target binding affinity. Moreover, the fluorine atom enhances lipophilicity, making it an attractive candidate for drug design.

In the realm of materials science, 4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol has been investigated for its role in synthesizing high-performance polymers. Its ability to undergo polymerization under specific conditions has led to the development of materials with improved thermal stability and mechanical properties. These polymers are being considered for use in advanced electronics and aerospace applications.

Recent research has also focused on the environmental impact of this compound. Studies have demonstrated its biodegradability under controlled conditions, which is a critical factor for its sustainable use in industrial processes. Additionally, its low toxicity profile makes it suitable for applications where human exposure is a concern.

The synthesis of 4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol involves multi-step organic reactions, including nucleophilic aromatic substitution and oxidation processes. Innovations in catalytic methods have significantly improved the yield and purity of this compound, making it more accessible for large-scale production.

In conclusion, 4-(4-Fluoro-2-hydroxyphenyl)-2-methoxyphenol (CAS No. 1261919-61-2) stands out as a versatile compound with diverse applications across multiple disciplines. Its unique chemical properties, combined with recent research advancements, position it as a key player in future scientific developments.

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