Cas no 1214341-66-8 (2-fluoro-5-(2-fluorophenyl)phenol)

2-Fluoro-5-(2-fluorophenyl)phenol is a fluorinated phenolic compound characterized by its bifunctional aromatic structure, incorporating two distinct fluorine substituents. This arrangement enhances its reactivity and utility as an intermediate in pharmaceutical and agrochemical synthesis. The presence of fluorine atoms improves metabolic stability and lipophilicity, making it valuable for designing bioactive molecules. Its phenol group allows for further functionalization, such as etherification or coupling reactions, while the fluorinated phenyl rings contribute to electronic modulation in target compounds. The compound exhibits high purity and consistent performance, ensuring reliability in complex synthetic pathways. Its structural features make it particularly useful in medicinal chemistry for developing fluorinated analogs with optimized pharmacokinetic properties.
2-fluoro-5-(2-fluorophenyl)phenol structure
1214341-66-8 structure
Product Name:2-fluoro-5-(2-fluorophenyl)phenol
CAS No:1214341-66-8
MF:C12H8F2O
MW:206.188130378723
MDL:MFCD14699563
CID:2617582
PubChem ID:46312658
Update Time:2025-06-14

2-fluoro-5-(2-fluorophenyl)phenol Chemical and Physical Properties

Names and Identifiers

    • 2-fluoro-5-(2-fluorophenyl)phenol
    • DTXSID00673374
    • 5-(2-FLUOROPHENYL)-2-FLUOROPHENOL
    • MFCD14699563
    • 2',4-Difluoro[1,1'-biphenyl]-3-ol
    • 5-(2-Fluorophenyl)-2-fluorophenol, 95%
    • 1214341-66-8
    • 2',4-Difluoro-[1,1'-biphenyl]-3-ol
    • FGA86151
    • MDL: MFCD14699563
    • Inchi: 1S/C12H8F2O/c13-10-4-2-1-3-9(10)8-5-6-11(14)12(15)7-8/h1-7,15H
    • InChI Key: YHGGIBYOGGRCCH-UHFFFAOYSA-N
    • SMILES: FC1C=CC=CC=1C1C=CC(=C(C=1)O)F

Computed Properties

  • Exact Mass: 206.05432120g/mol
  • Monoisotopic Mass: 206.05432120g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 1
  • Complexity: 210
  • 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: 3.8
  • Topological Polar Surface Area: 20.2?2

2-fluoro-5-(2-fluorophenyl)phenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB319580-5 g
5-(2-Fluorophenyl)-2-fluorophenol, 95%; .
1214341-66-8 95%
5g
€1159.00 2023-04-26
Alichem
A011001856-250mg
2',4-Difluorobiphenyl-3-ol
1214341-66-8 97%
250mg
$494.40 2023-09-04
Alichem
A011001856-500mg
2',4-Difluorobiphenyl-3-ol
1214341-66-8 97%
500mg
$831.30 2023-09-04
Alichem
A011001856-1g
2',4-Difluorobiphenyl-3-ol
1214341-66-8 97%
1g
$1445.30 2023-09-04
abcr
AB319580-5g
5-(2-Fluorophenyl)-2-fluorophenol, 95%; .
1214341-66-8 95%
5g
€1159.00 2025-03-19
Ambeed
A305002-1g
2',4-Difluoro-[1,1'-biphenyl]-3-ol
1214341-66-8 97%
1g
$254.0 2024-04-25
Ambeed
A305002-5g
2',4-Difluoro-[1,1'-biphenyl]-3-ol
1214341-66-8 97%
5g
$760.0 2024-04-25

Additional information on 2-fluoro-5-(2-fluorophenyl)phenol

Recent Advances in the Study of 2-Fluoro-5-(2-fluorophenyl)phenol (CAS: 1214341-66-8) in Chemical Biology and Pharmaceutical Research

2-Fluoro-5-(2-fluorophenyl)phenol (CAS: 1214341-66-8) is a fluorinated phenolic compound that has recently garnered significant attention in chemical biology and pharmaceutical research due to its unique structural properties and potential therapeutic applications. This compound, characterized by the presence of two fluorine atoms on its aromatic rings, exhibits enhanced stability and bioavailability, making it a promising candidate for drug development. Recent studies have explored its role as an intermediate in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and other targeted therapies.

One of the key areas of interest is the compound's utility in the synthesis of small-molecule inhibitors targeting protein kinases, which are critical regulators of cellular signaling pathways. A 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of 2-fluoro-5-(2-fluorophenyl)phenol exhibit potent inhibitory activity against specific kinases involved in cancer progression. The study highlighted the compound's ability to modulate kinase activity through selective binding to the ATP-binding site, thereby offering a potential avenue for the development of novel anticancer agents.

In addition to its applications in oncology, 2-fluoro-5-(2-fluorophenyl)phenol has also been investigated for its potential in neurodegenerative disease research. A recent preprint on bioRxiv reported that fluorinated phenolic compounds, including 1214341-66-8, exhibit neuroprotective effects in in vitro models of Alzheimer's disease. The researchers attributed these effects to the compound's ability to scavenge reactive oxygen species (ROS) and reduce oxidative stress, which are key contributors to neuronal damage in neurodegenerative disorders.

The synthetic pathways for 2-fluoro-5-(2-fluorophenyl)phenol have also been optimized in recent years, with a focus on improving yield and scalability. A 2022 publication in Organic Process Research & Development detailed a novel catalytic method for the fluorination of phenolic compounds, which significantly reduced the use of hazardous reagents and improved the overall efficiency of the synthesis. This advancement is particularly relevant for industrial-scale production, where cost-effectiveness and environmental considerations are paramount.

Despite these promising developments, challenges remain in the clinical translation of 2-fluoro-5-(2-fluorophenyl)phenol-based therapeutics. Pharmacokinetic studies have revealed variability in the compound's metabolic stability across different biological systems, necessitating further optimization of its chemical structure. Ongoing research aims to address these limitations by exploring structural analogs and prodrug strategies to enhance bioavailability and reduce off-target effects.

In conclusion, 2-fluoro-5-(2-fluorophenyl)phenol (CAS: 1214341-66-8) represents a versatile and promising scaffold in chemical biology and drug discovery. Its applications span from oncology to neurodegenerative diseases, and recent advancements in synthetic chemistry have further bolstered its potential for therapeutic development. Future research should focus on overcoming pharmacokinetic challenges and expanding the compound's utility in targeted therapies, paving the way for its eventual clinical application.

Recommended suppliers
Henan Dongyan Pharmaceutical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Henan Dongyan Pharmaceutical Co., Ltd
Jiangxi Boyang Pharmaceutical Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jiangxi Boyang Pharmaceutical Chemical Co., Ltd
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Hunan Well Medicine Synthesis Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Hunan Well Medicine Synthesis Technology Co., Ltd.
Zouping Mingyuan Import and Export Trading Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Zouping Mingyuan Import and Export Trading Co., Ltd