Cas no 1261955-34-3 (4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol)

4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol is a substituted phenolic compound featuring both chloro and methoxy functional groups, which contribute to its unique reactivity and potential applications in organic synthesis. The presence of electron-donating methoxy groups and an electron-withdrawing chlorine atom on the aromatic ring system enhances its versatility as an intermediate in pharmaceutical and agrochemical manufacturing. Its structural properties may facilitate selective functionalization, making it valuable for constructing complex molecules. The compound's stability under standard conditions ensures reliable handling and storage. Further research may explore its utility in catalysis, material science, or bioactive compound development.
4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol structure
1261955-34-3 structure
Product Name:4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol
CAS No:1261955-34-3
MF:C14H13ClO3
MW:264.704223394394
MDL:MFCD18315245
CID:2765854
PubChem ID:53220985
Update Time:2025-11-01

4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol Chemical and Physical Properties

Names and Identifiers

    • DTXSID60685670
    • 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol, 95%
    • 2'-Chloro-3,5'-dimethoxy[1,1'-biphenyl]-4-ol
    • 4-(2-CHLORO-5-METHOXYPHENYL)-2-METHOXYPHENOL
    • 1261955-34-3
    • MFCD18315245
    • 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol
    • MDL: MFCD18315245
    • Inchi: 1S/C14H13ClO3/c1-17-10-4-5-12(15)11(8-10)9-3-6-13(16)14(7-9)18-2/h3-8,16H,1-2H3
    • InChI Key: WEKQRFKKXOOVKM-UHFFFAOYSA-N
    • SMILES: ClC1=CC=C(C=C1C1C=CC(=C(C=1)OC)O)OC

Computed Properties

  • Exact Mass: 264.0553220Da
  • Monoisotopic Mass: 264.0553220Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 3
  • Complexity: 261
  • 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: 3.9
  • Topological Polar Surface Area: 38.7?2

4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB321424-5 g
4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol, 95%; .
1261955-34-3 95%
5g
€1159.00 2023-04-26
abcr
AB321424-5g
4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol, 95%; .
1261955-34-3 95%
5g
€1159.00 2025-03-19

Additional information on 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol

Comprehensive Overview of 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol (CAS No. 1261955-34-3)

4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol, with the CAS number 1261955-34-3, is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique phenolic and methoxy functional groups, serves as a critical intermediate in the synthesis of bioactive molecules. Its structural features, including the chloro and methoxy substituents, contribute to its versatility in chemical reactions, making it a valuable asset in modern synthetic chemistry.

In recent years, the demand for 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol has surged due to its potential applications in drug discovery and material science. Researchers are particularly interested in its role as a building block for antioxidant and anti-inflammatory agents, aligning with the growing focus on health and wellness. The compound's ability to modulate oxidative stress pathways has made it a subject of study in neurodegenerative disease research, a hot topic in the scientific community.

The synthesis of CAS 1261955-34-3 involves multi-step organic reactions, often starting from readily available precursors like guaiacol and chloroanisole derivatives. Advanced techniques such as HPLC and NMR spectroscopy are employed to ensure high purity and precise characterization. This meticulous process underscores the compound's importance in high-value applications, where even minor impurities can significantly impact performance.

From an industrial perspective, 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol is increasingly used in the development of specialty chemicals for agriculture. Its structural motifs are found in certain plant growth regulators and pesticide intermediates, addressing the global need for sustainable crop protection solutions. This aligns with current trends in green chemistry and eco-friendly agrochemicals, topics frequently searched by professionals in the field.

Quality control for 1261955-34-3 adheres to stringent international standards, with manufacturers providing detailed certificates of analysis (CoA) that include parameters like melting point, solubility, and chromatographic purity. These specifications are crucial for researchers who require consistent performance in their experiments, particularly in high-throughput screening environments.

The stability profile of 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol under various storage conditions has been extensively studied. Proper handling recommendations include protection from light and moisture, with optimal storage in amber glass containers at controlled temperatures. These preservation methods ensure the compound maintains its integrity for extended periods, a critical factor for long-term research projects.

In the context of intellectual property, several patents reference CAS 1261955-34-3 as a key intermediate in novel compound libraries. This reflects the growing importance of structure-activity relationship (SAR) studies in medicinal chemistry, where subtle modifications to such building blocks can lead to breakthrough therapeutics. The compound's patent landscape is frequently analyzed by competitive intelligence teams in the pharmaceutical industry.

Environmental considerations for 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol include its biodegradability profile and ecotoxicological data, which are increasingly important in regulatory submissions. Modern laboratories prioritize compounds with favorable environmental footprints, driving innovation in benign-by-design chemical development. This aligns with the principles of circular chemistry, another trending topic in scientific discourse.

From a market perspective, the global availability of 1261955-34-3 has expanded significantly, with specialized chemical suppliers offering custom synthesis services and bulk quantities. Procurement professionals often search for reliable suppliers of this compound, emphasizing the need for transparent supply chains and quality assurance documentation. The compound's pricing trends reflect its niche application status and the complexity of its synthesis.

Future research directions for 4-(2-Chloro-5-methoxyphenyl)-2-methoxyphenol may explore its potential in catalysis and material science applications, particularly in the development of advanced polymers with specific electronic properties. The compound's aromatic system and substituent pattern make it an interesting candidate for organic electronics, a field experiencing rapid growth. Such interdisciplinary applications demonstrate the compound's versatility beyond traditional pharmaceutical uses.

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