Cas no 1261911-91-4 (2-Cyano-4-(2,4-dimethoxyphenyl)phenol)

2-Cyano-4-(2,4-dimethoxyphenyl)phenol is a synthetic organic compound featuring a phenol core substituted with a cyano group and a 2,4-dimethoxyphenyl moiety. This structure imparts unique electronic and steric properties, making it valuable as an intermediate in pharmaceutical and agrochemical synthesis. The electron-withdrawing cyano group enhances reactivity in nucleophilic substitution reactions, while the dimethoxyphenyl substituent contributes to solubility in organic solvents. Its well-defined molecular architecture allows for precise functionalization, facilitating the development of complex molecules. The compound’s stability under mild conditions and compatibility with diverse reaction pathways underscore its utility in fine chemical applications. Analytical methods confirm high purity, ensuring reproducibility in research and industrial processes.
2-Cyano-4-(2,4-dimethoxyphenyl)phenol structure
1261911-91-4 structure
Product Name:2-Cyano-4-(2,4-dimethoxyphenyl)phenol
CAS No:1261911-91-4
MF:C15H13NO3
MW:255.268624067307
MDL:MFCD18314402
CID:2621831
PubChem ID:53220077
Update Time:2025-05-22

2-Cyano-4-(2,4-dimethoxyphenyl)phenol Chemical and Physical Properties

Names and Identifiers

    • 1261911-91-4
    • 2-CYANO-4-(2,4-DIMETHOXYPHENYL)PHENOL
    • AKOS017557737
    • 4-Hydroxy-2',4'-dimethoxy[1,1'-biphenyl]-3-carbonitrile
    • 2-Cyano-4-(2,4-dimethoxyphenyl)phenol, 95%
    • MFCD18314402
    • DTXSID50684854
    • 2-Cyano-4-(2,4-dimethoxyphenyl)phenol
    • MDL: MFCD18314402
    • Inchi: 1S/C15H13NO3/c1-18-12-4-5-13(15(8-12)19-2)10-3-6-14(17)11(7-10)9-16/h3-8,17H,1-2H3
    • InChI Key: DAWJQNOTQWGIEG-UHFFFAOYSA-N
    • SMILES: O(C)C1C=C(C=CC=1C1C=CC(=C(C#N)C=1)O)OC

Computed Properties

  • Exact Mass: 255.08954328Da
  • Monoisotopic Mass: 255.08954328Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 3
  • Complexity: 338
  • 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: 3.4
  • Topological Polar Surface Area: 62.5?2

2-Cyano-4-(2,4-dimethoxyphenyl)phenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB320445-5 g
2-Cyano-4-(2,4-dimethoxyphenyl)phenol, 95%; .
1261911-91-4 95%
5g
€1159.00 2023-04-26
abcr
AB320445-5g
2-Cyano-4-(2,4-dimethoxyphenyl)phenol, 95%; .
1261911-91-4 95%
5g
€1159.00 2025-04-21

Additional information on 2-Cyano-4-(2,4-dimethoxyphenyl)phenol

Comprehensive Overview of 2-Cyano-4-(2,4-dimethoxyphenyl)phenol (CAS No. 1261911-91-4)

2-Cyano-4-(2,4-dimethoxyphenyl)phenol (CAS No. 1261911-91-4) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research due to its unique molecular structure. The compound features a cyano group and dimethoxyphenyl substituents, which contribute to its potential applications in drug discovery and material science. Researchers are particularly interested in its role as an intermediate in synthesizing bioactive molecules, given its ability to modulate electronic and steric properties.

In recent years, the demand for high-purity intermediates like 2-Cyano-4-(2,4-dimethoxyphenyl)phenol has surged, driven by advancements in precision medicine and green chemistry. This compound’s structural versatility makes it a candidate for developing novel antioxidants and UV stabilizers, aligning with the growing focus on sustainable and eco-friendly additives. Its CAS No. 1261911-91-4 is frequently searched in academic databases, reflecting its relevance in cutting-edge research.

From a synthetic perspective, 2-Cyano-4-(2,4-dimethoxyphenyl)phenol is synthesized via multistep organic reactions, often involving Pd-catalyzed cross-coupling or nucleophilic aromatic substitution. Its electron-withdrawing cyano group enhances reactivity, enabling diverse functionalizations. This property is leveraged in designing small-molecule inhibitors for enzymatic studies, a hot topic in cancer therapeutics and neurodegenerative disease research.

The compound’s solubility and stability profiles are critical for formulation scientists. Studies indicate that 2-Cyano-4-(2,4-dimethoxyphenyl)phenol exhibits moderate solubility in polar organic solvents, making it suitable for high-throughput screening assays. Its thermal stability further supports its use in polymer coatings and electronic materials, areas where users often inquire about heat-resistant additives.

Analytical characterization of CAS No. 1261911-91-4 typically involves HPLC, NMR, and mass spectrometry, ensuring compliance with Good Manufacturing Practices (GMP). Quality control is paramount, as impurities can affect downstream applications. This aligns with industry trends emphasizing traceability and regulatory compliance, frequently searched terms in pharmaceutical supply chains.

Beyond industrial applications, 2-Cyano-4-(2,4-dimethoxyphenyl)phenol is explored in academic labs for its photophysical properties. Its fluorescence quenching behavior is investigated for sensor development, a trending topic in environmental monitoring. Users searching for “advanced organic sensors” or “l(fā)uminescent probes” will find this compound’s derivatives highly relevant.

In summary, 2-Cyano-4-(2,4-dimethoxyphenyl)phenol (CAS No. 1261911-91-4) bridges multiple disciplines, from medicinal chemistry to material engineering. Its custom synthesis and scalability remain key discussion points, addressing queries like “bulk suppliers of specialty phenols”. As research evolves, this compound is poised to play a pivotal role in next-generation innovations.

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