Cas no 1261927-24-5 (2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid)

2-(3-Fluoro-5-hydroxyphenyl)-6-methylbenzoic acid is a fluorinated aromatic carboxylic acid derivative with a hydroxyl substituent, offering unique reactivity and structural properties for synthetic applications. The presence of both fluorine and hydroxyl groups enhances its potential as an intermediate in pharmaceutical and agrochemical synthesis, where selective functionalization is critical. The methyl group at the 6-position contributes to steric and electronic modulation, influencing regioselectivity in further derivatization. This compound’s balanced polarity and stability make it suitable for use in cross-coupling reactions, metal-catalyzed transformations, or as a scaffold for bioactive molecule development. Its well-defined structure ensures reproducibility in research and industrial processes.
2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid structure
1261927-24-5 structure
Product Name:2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid
CAS No:1261927-24-5
MF:C14H11FO3
MW:246.233747720718
MDL:MFCD18319727
CID:1219237
PubChem ID:53225645
Update Time:2025-10-22

2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid Chemical and Physical Properties

Names and Identifiers

    • 2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid
    • MFCD18319727
    • DTXSID80689377
    • 1261927-24-5
    • 2-(3-Fluoro-5-hydroxyphenyl)-6-methylbenzoic acid, 95%
    • 3'-Fluoro-5'-hydroxy-3-methyl[1,1'-biphenyl]-2-carboxylic acid
    • MDL: MFCD18319727
    • Inchi: 1S/C14H11FO3/c1-8-3-2-4-12(13(8)14(17)18)9-5-10(15)7-11(16)6-9/h2-7,16H,1H3,(H,17,18)
    • InChI Key: QNRWNBUHHSHVJV-UHFFFAOYSA-N
    • SMILES: FC1C=C(C=C(C=1)C1C=CC=C(C)C=1C(=O)O)O

Computed Properties

  • Exact Mass: 246.06922237g/mol
  • Monoisotopic Mass: 246.06922237g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 2
  • Complexity: 307
  • 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: 3.2
  • Topological Polar Surface Area: 57.5?2

2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB326807-5 g
2-(3-Fluoro-5-hydroxyphenyl)-6-methylbenzoic acid, 95%; .
1261927-24-5 95%
5g
€1159.00 2023-04-26
abcr
AB326807-5g
2-(3-Fluoro-5-hydroxyphenyl)-6-methylbenzoic acid, 95%; .
1261927-24-5 95%
5g
€1159.00 2024-06-08

Additional information on 2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid

Comprehensive Overview of 2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid (CAS No. 1261927-24-5)

2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid (CAS No. 1261927-24-5) is a fluorinated aromatic carboxylic acid derivative that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique fluoro-hydroxyphenyl and methylbenzoic acid structural motifs, exhibits potential applications in drug discovery and material science. Its molecular formula, C14H11FO3, and precise structural features make it a valuable intermediate for synthesizing bioactive molecules.

In recent years, the demand for fluorinated organic compounds like 2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid has surged due to their enhanced metabolic stability and bioavailability. Researchers are particularly interested in its role as a building block for small-molecule inhibitors targeting enzymes such as kinases and proteases. The presence of both hydroxyl and carboxylic acid functional groups allows for versatile chemical modifications, enabling the development of derivatives with tailored properties.

The synthesis of CAS No. 1261927-24-5 typically involves multi-step organic reactions, including Friedel-Crafts acylation and halogenation. Advanced analytical techniques like NMR spectroscopy and high-resolution mass spectrometry are employed to confirm its purity and structural integrity. Given its potential in medicinal chemistry, this compound is often explored in the context of anti-inflammatory and neuroprotective agents, aligning with current trends in precision medicine.

From an industrial perspective, 2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid is also investigated for its utility in advanced material synthesis. Its aromatic backbone and polar functional groups make it a candidate for designing polymeric materials with specific thermal or optical properties. Environmental considerations, such as green chemistry principles, are increasingly applied to its production to minimize waste and energy consumption.

Frequently asked questions about this compound include its solubility profile (e.g., in DMSO or ethanol), storage conditions (typically 2–8°C under inert atmosphere), and handling precautions (use of personal protective equipment). As interest grows in sustainable chemistry, researchers are also exploring biocatalytic routes to synthesize fluorinated benzoic acids like this one, reducing reliance on traditional halogenation methods.

In summary, 2-(3-fluoro-5-hydroxyphenyl)-6-methylbenzoic Acid (CAS No. 1261927-24-5) represents a versatile scaffold with broad applicability in pharmaceuticals, agrochemicals, and material science. Its combination of fluorine and hydroxyl substituents offers unique opportunities for innovation, particularly in addressing challenges like drug resistance and material durability. Ongoing research continues to uncover new dimensions of its utility, solidifying its importance in modern chemistry.

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