Cas no 1261951-48-7 (2-Chloro-5-(4-methoxy-2-methylphenyl)phenol)

2-Chloro-5-(4-methoxy-2-methylphenyl)phenol is a substituted phenolic compound featuring a chloro group at the 2-position and a 4-methoxy-2-methylphenyl moiety at the 5-position of the phenol ring. This structural configuration imparts distinct chemical properties, making it a valuable intermediate in organic synthesis, particularly for pharmaceuticals and agrochemicals. The presence of electron-donating (methoxy) and electron-withdrawing (chloro) groups enhances its reactivity in electrophilic and nucleophilic substitution reactions. Its stability under various conditions and compatibility with further functionalization make it suitable for complex molecular frameworks. The compound is typically handled under controlled conditions due to its phenolic nature, ensuring optimal purity and performance in synthetic applications.
2-Chloro-5-(4-methoxy-2-methylphenyl)phenol structure
1261951-48-7 structure
Product Name:2-Chloro-5-(4-methoxy-2-methylphenyl)phenol
CAS No:1261951-48-7
MF:C14H13ClO2
MW:248.704823255539
MDL:MFCD18315571
CID:2621880
PubChem ID:53221307
Update Time:2025-08-02

2-Chloro-5-(4-methoxy-2-methylphenyl)phenol Chemical and Physical Properties

Names and Identifiers

    • AKOS017558291
    • 2-CHLORO-5-(4-METHOXY-2-METHYLPHENYL)PHENOL
    • 4-Chloro-4'-methoxy-2'-methyl[1,1'-biphenyl]-3-ol
    • 1261951-48-7
    • DTXSID90685966
    • MFCD18315571
    • 2-Chloro-5-(4-methoxy-2-methylphenyl)phenol, 95%
    • 2-Chloro-5-(4-methoxy-2-methylphenyl)phenol
    • MDL: MFCD18315571
    • Inchi: 1S/C14H13ClO2/c1-9-7-11(17-2)4-5-12(9)10-3-6-13(15)14(16)8-10/h3-8,16H,1-2H3
    • InChI Key: FRZRYMXVJGRHNE-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=CC=1O)C1C=CC(=CC=1C)OC

Computed Properties

  • Exact Mass: 248.0604073Da
  • Monoisotopic Mass: 248.0604073Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 2
  • Complexity: 246
  • 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: 4.2
  • Topological Polar Surface Area: 29.5?2

2-Chloro-5-(4-methoxy-2-methylphenyl)phenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB321772-5 g
2-Chloro-5-(4-methoxy-2-methylphenyl)phenol, 95%; .
1261951-48-7 95%
5g
€1159.00 2023-04-26
abcr
AB321772-5g
2-Chloro-5-(4-methoxy-2-methylphenyl)phenol, 95%; .
1261951-48-7 95%
5g
€1159.00 2025-03-19

Additional information on 2-Chloro-5-(4-methoxy-2-methylphenyl)phenol

Comprehensive Overview of 2-Chloro-5-(4-methoxy-2-methylphenyl)phenol (CAS No. 1261951-48-7): Properties, Applications, and Industry Insights

2-Chloro-5-(4-methoxy-2-methylphenyl)phenol (CAS No. 1261951-48-7) is a specialized organic compound gaining attention in pharmaceutical and agrochemical research due to its unique structural properties. This chlorinated phenolic derivative features a methoxy-methylphenyl substitution pattern, which contributes to its potential as an intermediate in synthetic chemistry. The compound's molecular formula C14H13ClO2 and precise chemical structure make it valuable for developing novel bioactive molecules.

Recent studies highlight the growing demand for halogenated phenolic compounds in medicinal chemistry, particularly for their antimicrobial and antioxidant properties. Researchers are investigating CAS 1261951-48-7 as a potential building block for drug discovery, especially in designing selective enzyme inhibitors. The compound's lipophilic character and electron-rich aromatic system enable interesting interactions with biological targets, making it relevant to current trends in precision medicine and targeted therapeutics.

From an industrial perspective, 2-Chloro-5-(4-methoxy-2-methylphenyl)phenol demonstrates excellent stability under various processing conditions, which explains its emerging applications in specialty chemicals manufacturing. Quality control parameters for this compound typically include HPLC purity (>98%), specific melting point range (observed between 112-115°C), and characteristic spectroscopic fingerprints (IR, NMR, and mass spectra). These specifications ensure batch-to-batch consistency for research and development purposes.

The synthesis of CAS 1261951-48-7 typically involves multi-step organic reactions starting from commercially available precursors. Modern green chemistry approaches are being adapted to optimize its production, addressing industry concerns about sustainable manufacturing. Recent patent literature suggests innovative catalytic methods that improve yield while reducing environmental impact—a response to growing market demand for eco-friendly synthetic routes.

Analytical characterization of 2-Chloro-5-(4-methoxy-2-methylphenyl)phenol reveals important structure-activity relationships that guide its applications. The electron-donating methoxy group at the para position and steric effects from the ortho-methyl substitution create distinct electronic properties. These features are particularly valuable when designing molecular probes for biochemical studies or developing functional materials with specific optical properties.

Market analysts note increasing interest in CAS 1261951-48-7 from Asia-Pacific research institutions, coinciding with regional investments in innovative chemical entities. The compound's structure-optimization potential makes it attractive for fragment-based drug discovery—a hot topic in computational chemistry circles. Several recent publications have explored its molecular docking characteristics against various protein targets, demonstrating its versatility in rational drug design methodologies.

Storage and handling recommendations for 2-Chloro-5-(4-methoxy-2-methylphenyl)phenol emphasize protection from light and moisture, with optimal stability observed at controlled room temperature. These protocols align with standard practices for aromatic chlorinated compounds, ensuring material integrity during transportation and long-term storage. Proper chemical compatibility assessments are recommended when formulating this compound with other substances.

Future research directions for CAS 1261951-48-7 may explore its potential in material science applications, particularly as a monomer for specialized polymers or as a component in advanced coating systems. The compound's balanced hydrophobic-hydrophilic properties suggest possible utility in surface modification technologies, an area experiencing rapid growth across multiple industries. Continued investigation of its physicochemical behavior under different conditions will further elucidate its full commercial potential.

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