Cas no 1184537-99-2 (2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid)

2-Fluoro-5-(4-methoxy-3-methylphenyl)benzoic acid is a fluorinated benzoic acid derivative featuring a methoxy- and methyl-substituted phenyl ring at the 5-position. This compound is of interest in pharmaceutical and agrochemical research due to its potential as a synthetic intermediate for bioactive molecules. The fluorine substituent enhances metabolic stability and binding affinity, while the methoxy and methyl groups contribute to steric and electronic modulation. Its well-defined structure allows for precise functionalization in medicinal chemistry applications. The acid functionality facilitates further derivatization, making it a versatile building block for the development of novel compounds. High purity and consistent synthesis ensure reliability in research and industrial applications.
2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid structure
1184537-99-2 structure
Product Name:2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid
CAS No:1184537-99-2
MF:C15H13FO3
MW:260.260328054428
MDL:MFCD12859524
CID:1207510
PubChem ID:53211253
Update Time:2025-10-28

2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid Chemical and Physical Properties

Names and Identifiers

    • 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid
    • AKOS005820807
    • 2-Fluoro-5-(4-methoxy-3-methylphenyl)benzoic acid, 95%
    • 4-Fluoro-4'-methoxy-3'-methyl[1,1'-biphenyl]-3-carboxylic acid
    • MFCD12859524
    • DTXSID70681284
    • 1184537-99-2
    • MDL: MFCD12859524
    • Inchi: 1S/C15H13FO3/c1-9-7-10(4-6-14(9)19-2)11-3-5-13(16)12(8-11)15(17)18/h3-8H,1-2H3,(H,17,18)
    • InChI Key: FWVLPAPEEOZMPL-UHFFFAOYSA-N
    • SMILES: FC1C=CC(=CC=1C(=O)O)C1=CC=C(C(C)=C1)OC

Computed Properties

  • Exact Mass: 260.08487243g/mol
  • Monoisotopic Mass: 260.08487243g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 3
  • Complexity: 321
  • 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: 3.5
  • Topological Polar Surface Area: 46.5?2

2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB327552-5 g
2-Fluoro-5-(4-methoxy-3-methylphenyl)benzoic acid, 95%; .
1184537-99-2 95%
5g
€1159.00 2023-04-26
abcr
AB327552-5g
2-Fluoro-5-(4-methoxy-3-methylphenyl)benzoic acid, 95%; .
1184537-99-2 95%
5g
€1159.00 2025-04-22

2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid Related Literature

Additional information on 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid

Recent Advances in the Study of 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid (CAS: 1184537-99-2)

The compound 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid (CAS: 1184537-99-2) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its unique structural features, has shown promising potential in various therapeutic applications. Recent studies have focused on its synthesis, pharmacological properties, and mechanisms of action, providing valuable insights for drug development.

One of the key areas of research has been the optimization of synthetic routes for 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid. A study published in the Journal of Medicinal Chemistry (2023) demonstrated an efficient multi-step synthesis protocol that improved yield and purity. The protocol involved the use of palladium-catalyzed cross-coupling reactions, followed by selective fluorination and carboxylation steps. This advancement is critical for scaling up production for preclinical and clinical studies.

Pharmacological evaluations have revealed that 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid exhibits potent anti-inflammatory and analgesic properties. In vitro studies using human cell lines indicated that the compound inhibits cyclooxygenase-2 (COX-2) activity with high selectivity, suggesting its potential as a next-generation non-steroidal anti-inflammatory drug (NSAID). Furthermore, in vivo studies in rodent models confirmed its efficacy in reducing inflammation and pain with minimal gastrointestinal side effects, a common limitation of traditional NSAIDs.

Another groundbreaking study explored the compound's role in oncology. Researchers found that 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid acts as a modulator of the tumor microenvironment by inhibiting specific signaling pathways involved in angiogenesis and metastasis. These findings, published in Cancer Research (2024), highlight the compound's dual functionality as both an anti-inflammatory and anti-cancer agent, opening new avenues for combination therapies.

Despite these promising results, challenges remain in the clinical translation of 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid. Pharmacokinetic studies have identified issues related to bioavailability and metabolic stability, which are currently being addressed through structural modifications and formulation strategies. Collaborative efforts between academic institutions and pharmaceutical companies are underway to overcome these hurdles and accelerate the compound's progression to clinical trials.

In conclusion, 2-fluoro-5-(4-methoxy-3-methylphenyl)benzoic Acid (CAS: 1184537-99-2) represents a versatile and promising candidate in the field of medicinal chemistry. Its multifaceted pharmacological profile, combined with recent advancements in synthesis and mechanistic understanding, positions it as a valuable asset for future drug development. Continued research and collaboration will be essential to fully realize its therapeutic potential.

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