Cas no 1261898-32-1 (6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol)

6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol is a specialized aromatic compound featuring a chloro-substituted phenyl ring, a methoxycarbonyl group, and a formylphenol moiety. Its unique structure makes it valuable as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. The presence of both formyl and hydroxyl groups enhances its reactivity, enabling selective functionalization for complex molecular frameworks. The chloro and methoxycarbonyl substituents further contribute to its versatility in cross-coupling and condensation reactions. This compound is characterized by high purity and stability, ensuring reliable performance in synthetic applications. Its well-defined structure facilitates precise modifications, making it a useful building block in advanced chemical research and industrial processes.
6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol structure
1261898-32-1 structure
Product Name:6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol
CAS No:1261898-32-1
MF:C15H11ClO4
MW:290.698443651199
MDL:MFCD18314880
CID:2762072
PubChem ID:53220626
Update Time:2025-06-09

6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol Chemical and Physical Properties

Names and Identifiers

    • MFCD18314880
    • DTXSID00685356
    • 6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol, 95%
    • 6-(2-CHLORO-5-METHOXYCARBONYLPHENYL)-2-FORMYLPHENOL
    • Methyl 6-chloro-3'-formyl-2'-hydroxy[1,1'-biphenyl]-3-carboxylate
    • 1261898-32-1
    • 6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol
    • MDL： MFCD18314880
    • Inchi： 1S/C15H11ClO4/c1-20-15(19)9-5-6-13(16)12(7-9)11-4-2-3-10(8-17)14(11)18/h2-8,18H,1H3
    • InChI Key： UEGOJUOUYWSIHS-UHFFFAOYSA-N
    • SMILES： ClC1=CC=C(C(=O)OC)C=C1C1C=CC=C(C=O)C=1O

Computed Properties

  • Exact Mass: 290.0345865Da
  • Monoisotopic Mass: 290.0345865Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 4
  • Complexity: 360
  • 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: 3.7
  • Topological Polar Surface Area: 63.6?2

6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB321054-5 g
6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol, 95%; .
 1261898-32-1 95%
5g
 €1159.00 2023-04-26
abcr
AB321054-5g
6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol, 95%; .
 1261898-32-1 95%
5g
 €1159.00 2025-02-21

6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol Related Literature

Additional information on 6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol

Comprehensive Overview of 6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261898-32-1)

6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261898-32-1) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its unique phenolic and carbonyl functional groups, serves as a versatile intermediate in the synthesis of complex molecules. Its molecular structure, featuring a chloro substituent and a methoxycarbonyl group, makes it particularly valuable for applications requiring precise chemical modifications.

In recent years, the demand for high-purity intermediates like 6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol has surged, driven by advancements in drug discovery and material science. Researchers are increasingly exploring its potential in designing targeted therapies and sustainable agrochemicals. The compound's formyl group offers reactivity that is crucial for cross-coupling reactions, a topic frequently searched in academic and industrial circles.

One of the most discussed applications of CAS No. 1261898-32-1 is its role in photodynamic therapy (PDT), a cutting-edge treatment for certain medical conditions. The compound's ability to absorb specific wavelengths of light makes it a candidate for photosensitizer development. This aligns with the growing interest in non-invasive treatments and precision medicine, which dominate current healthcare trends.

From a synthetic chemistry perspective, 6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol is often highlighted in discussions about green chemistry. Its potential for use in catalyzed reactions with reduced environmental impact resonates with the global push for sustainable manufacturing. Searches for eco-friendly synthesis methods and biodegradable intermediates frequently reference compounds like this.

The compound's structural versatility also makes it a subject of interest in computational chemistry. Researchers utilize molecular modeling tools to predict its behavior in various chemical environments, a topic that has seen increased search volume due to the rise of AI-driven drug design. This intersection of experimental and theoretical chemistry underscores the compound's relevance in modern scientific inquiry.

Quality control and analytical characterization of CAS No. 1261898-32-1 are critical for ensuring its efficacy in downstream applications. Techniques such as HPLC, NMR spectroscopy, and mass spectrometry are commonly employed to verify its purity and structural integrity. These methods are frequently searched by professionals in the pharmaceutical and chemical industries, reflecting the compound's importance in high-stakes research.

In summary, 6-(2-Chloro-5-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261898-32-1) represents a critical building block in contemporary chemical research. Its applications span drug development, agrochemical innovation, and sustainable chemistry, making it a compound of enduring interest. As scientific advancements continue to unfold, this molecule is poised to play a pivotal role in addressing some of the most pressing challenges in healthcare and environmental sustainability.

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