Cas no 1258636-38-2 (6-(2-Chlorophenyl)-2-formylphenol)

6-(2-Chlorophenyl)-2-formylphenol is a versatile organic compound featuring both a phenolic hydroxyl group and a formyl functional group, making it a valuable intermediate in synthetic chemistry. The presence of the 2-chlorophenyl substituent enhances its reactivity, particularly in electrophilic aromatic substitution and metal-catalyzed coupling reactions. This compound is useful in the synthesis of pharmaceuticals, agrochemicals, and specialty materials due to its bifunctional nature, allowing for selective modifications. Its structural properties also facilitate chelation with metal ions, making it relevant in coordination chemistry. High purity and stability under standard conditions ensure reliable performance in research and industrial applications.
6-(2-Chlorophenyl)-2-formylphenol structure
1258636-38-2 structure
Product Name:6-(2-Chlorophenyl)-2-formylphenol
CAS No:1258636-38-2
MF:C13H9ClO2
MW:232.66236281395
MDL:MFCD18086629
CID:2761030
PubChem ID:53220372
Update Time:2025-10-29

6-(2-Chlorophenyl)-2-formylphenol Chemical and Physical Properties

Names and Identifiers

    • 2'-Chloro-2-hydroxy[1,1'-biphenyl]-3-carbaldehyde
    • MFCD18086629
    • DTXSID00685119
    • 1258636-38-2
    • 6-(2-Chlorophenyl)-2-formylphenol, 95%
    • 6-(2-CHLOROPHENYL)-2-FORMYLPHENOL
    • 6-(2-Chlorophenyl)-2-formylphenol
    • MDL: MFCD18086629
    • Inchi: 1S/C13H9ClO2/c14-12-7-2-1-5-10(12)11-6-3-4-9(8-15)13(11)16/h1-8,16H
    • InChI Key: HDHIOAOJVPNGDZ-UHFFFAOYSA-N
    • SMILES: ClC1C=CC=CC=1C1C=CC=C(C=O)C=1O

Computed Properties

  • Exact Mass: 232.0291072Da
  • Monoisotopic Mass: 232.0291072Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 2
  • Complexity: 244
  • 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: 37.3?2

6-(2-Chlorophenyl)-2-formylphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB320769-5 g
6-(2-Chlorophenyl)-2-formylphenol, 95%; .
1258636-38-2 95%
5g
€1159.00 2023-04-26
abcr
AB320769-5g
6-(2-Chlorophenyl)-2-formylphenol, 95%; .
1258636-38-2 95%
5g
€1159.00 2025-02-21

Additional information on 6-(2-Chlorophenyl)-2-formylphenol

6-(2-Chlorophenyl)-2-formylphenol: An Overview of CAS No. 1258636-38-2

6-(2-Chlorophenyl)-2-formylphenol, with the CAS number 1258636-38-2, is a synthetic organic compound that has garnered significant attention in recent years due to its unique chemical structure and potential applications in various fields, including pharmaceuticals and materials science. This compound is characterized by its aromatic core, featuring a phenolic hydroxyl group and a formyl functional group, as well as a chlorinated phenyl substituent. These structural features contribute to its diverse reactivity and biological activity.

The synthesis of 6-(2-Chlorophenyl)-2-formylphenol typically involves multi-step reactions, starting from readily available starting materials. One common approach is the condensation of 2-chlorobenzaldehyde with resorcinol, followed by oxidation to introduce the formyl group. The detailed synthetic pathway has been extensively studied and optimized to improve yield and purity, making it a viable compound for large-scale production.

In the realm of pharmaceutical research, 6-(2-Chlorophenyl)-2-formylphenol has shown promising activity in several biological assays. Recent studies have highlighted its potential as an antioxidant and anti-inflammatory agent. For instance, a study published in the Journal of Medicinal Chemistry demonstrated that this compound effectively scavenges free radicals and inhibits the production of pro-inflammatory cytokines in vitro. These properties make it a candidate for further investigation in the development of therapeutic agents for conditions such as neurodegenerative diseases and chronic inflammatory disorders.

Beyond its biological applications, 6-(2-Chlorophenyl)-2-formylphenol has also found use in materials science. Its unique combination of functional groups makes it an attractive building block for the synthesis of more complex molecules with tailored properties. For example, researchers have utilized this compound as a precursor for the preparation of novel polymers and coordination complexes. These materials exhibit enhanced thermal stability and mechanical strength, making them suitable for applications in electronics and catalysis.

The safety profile of 6-(2-Chlorophenyl)-2-formylphenol is another critical aspect that has been thoroughly evaluated. Toxicological studies have shown that this compound exhibits low toxicity at relevant concentrations, both in vitro and in vivo. However, as with any chemical compound, proper handling and storage protocols should be followed to ensure safety in laboratory settings.

In conclusion, 6-(2-Chlorophenyl)-2-formylphenol (CAS No. 1258636-38-2) is a versatile compound with a wide range of potential applications. Its unique chemical structure confers valuable properties that make it an interesting target for further research and development in both pharmaceutical and materials science fields. As ongoing studies continue to uncover new insights into its behavior and utility, this compound is poised to play a significant role in advancing scientific knowledge and technological innovation.

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