Cas no 1261888-38-3 (5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol)

5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol is a fluorinated aromatic compound featuring a methoxycarbonyl substituent and a phenolic hydroxyl group. Its structural design offers versatility in synthetic applications, particularly as an intermediate in pharmaceuticals and agrochemicals. The fluorine atom enhances metabolic stability and binding affinity, while the methoxycarbonyl group provides a reactive handle for further functionalization. The phenolic moiety allows for derivatization or coordination in metal-catalyzed reactions. This compound is valued for its potential in constructing complex molecular architectures with improved pharmacokinetic properties. Its well-defined reactivity profile makes it suitable for precision synthesis in medicinal chemistry and material science research.
5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol structure
1261888-38-3 structure
Product Name:5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol
CAS No:1261888-38-3
MF:C15H13FO3
MW:260.260328054428
MDL:MFCD18313410
CID:2761404
PubChem ID:53219103
Update Time:2025-05-19

5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol Chemical and Physical Properties

Names and Identifiers

    • MFCD18313410
    • 5-(2-FLUORO-4-METHOXYCARBONYLPHENYL)-3-METHYLPHENOL
    • DTXSID60683979
    • 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol, 95%
    • Methyl 2-fluoro-3'-hydroxy-5'-methyl[1,1'-biphenyl]-4-carboxylate
    • 1261888-38-3
    • 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol
    • MDL: MFCD18313410
    • Inchi: 1S/C15H13FO3/c1-9-5-11(7-12(17)6-9)13-4-3-10(8-14(13)16)15(18)19-2/h3-8,17H,1-2H3
    • InChI Key: JPLUUFYWSNFAHH-UHFFFAOYSA-N
    • SMILES: FC1C=C(C(=O)OC)C=CC=1C1C=C(C=C(C)C=1)O

Computed Properties

  • Exact Mass: 260.08487243Da
  • Monoisotopic Mass: 260.08487243Da
  • 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

5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB319423-5 g
5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol, 95%; .
1261888-38-3 95%
5g
€1,159.00 2022-08-31
abcr
AB319423-5g
5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol, 95%; .
1261888-38-3 95%
5g
€1159.00 2024-04-20

5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol Related Literature

Additional information on 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol

Comprehensive Overview of 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol (CAS No. 1261888-38-3)

5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol (CAS No. 1261888-38-3) is a specialized organic compound that has garnered significant attention in pharmaceutical and material science research. This compound, characterized by its unique fluorinated aromatic and methoxycarbonyl functional groups, serves as a versatile intermediate in the synthesis of advanced materials and bioactive molecules. Its molecular structure, which includes a phenol core substituted with a methyl group and a 2-fluoro-4-methoxycarbonylphenyl moiety, contributes to its distinct chemical properties and reactivity.

The growing interest in fluorinated compounds like 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol is driven by their applications in drug discovery and agrochemical development. Researchers are particularly intrigued by the role of fluorine substitution in enhancing metabolic stability and bioavailability, a topic frequently searched in academic and industrial circles. The compound’s methoxycarbonyl group further expands its utility, enabling its use in polymer chemistry and as a precursor for high-performance materials.

In pharmaceutical research, 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol is explored for its potential as a building block in the synthesis of small-molecule inhibitors and protease-targeting agents. Recent studies highlight its relevance in addressing challenges such as drug resistance and selective enzyme modulation, aligning with trending searches in medicinal chemistry. Additionally, its phenolic hydroxyl group offers opportunities for further functionalization, making it a valuable asset in combinatorial chemistry libraries.

The compound’s physicochemical properties, including its solubility, thermal stability, and reactivity under mild conditions, are frequently discussed in forums and publications. These attributes make it suitable for applications in organic electronics and catalysis, where precision and efficiency are paramount. Industry professionals often search for CAS No. 1261888-38-3 to source high-purity samples for experimental and commercial purposes.

From an environmental perspective, the demand for sustainable synthetic routes to compounds like 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol has risen, reflecting broader trends in green chemistry. Researchers are investigating catalyst-free and energy-efficient methods to produce this compound, addressing concerns about waste reduction and eco-friendly manufacturing. Such innovations are often highlighted in SEO-optimized content to attract environmentally conscious audiences.

Market analyses indicate a steady increase in the procurement of 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol, particularly from sectors focused on advanced material synthesis and pharmaceutical intermediates. Suppliers and distributors emphasize its high purity grade and batch consistency, which are critical for regulatory compliance and reproducibility in research. These factors contribute to its prominence in search queries related to specialty chemicals.

In summary, 5-(2-Fluoro-4-methoxycarbonylphenyl)-3-methylphenol (CAS No. 1261888-38-3) represents a compound of significant scientific and industrial value. Its multifaceted applications, coupled with ongoing research into its derivatives, ensure its relevance in cutting-edge fields. By integrating SEO-friendly keywords such as fluorinated aromatic intermediates and methoxycarbonylphenol derivatives, this overview aims to provide a resourceful and engaging read for chemists, researchers, and industry stakeholders alike.

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