Cas no 1261895-50-4 (6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol)

6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol is a versatile intermediate in organic synthesis, particularly valuable for its bifunctional reactivity due to the presence of both formyl and hydroxyl groups. The chloro and methoxycarbonyl substituents enhance its utility in cross-coupling reactions and further derivatization. This compound exhibits high purity and stability, making it suitable for pharmaceutical and fine chemical applications. Its structural features allow for precise modifications, facilitating the synthesis of complex molecules. The product is rigorously characterized to ensure consistency, meeting the demands of research and industrial processes requiring reliable building blocks for heterocyclic and aromatic systems.
6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol structure
1261895-50-4 structure
Product Name:6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol
CAS No:1261895-50-4
MF:C15H11ClO4
MW:290.698443651199
MDL:MFCD18314886
CID:2761881
PubChem ID:53220632
Update Time:2025-06-08

6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol Chemical and Physical Properties

Names and Identifiers

    • 1261895-50-4
    • Methyl 4-chloro-3'-formyl-2'-hydroxy-[1,1'-biphenyl]-3-carboxylate
    • Methyl 4-chloro-3'-formyl-2'-hydroxy[1,1'-biphenyl]-3-carboxylate
    • 6-(4-CHLORO-3-METHOXYCARBONYLPHENYL)-2-FORMYLPHENOL
    • DTXSID10685362
    • 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol, 95%
    • MFCD18314886
    • 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol
    • MDL: MFCD18314886
    • Inchi: 1S/C15H11ClO4/c1-20-15(19)12-7-9(5-6-13(12)16)11-4-2-3-10(8-17)14(11)18/h2-8,18H,1H3
    • InChI Key: DULGPQUNHYDKLE-UHFFFAOYSA-N
    • SMILES: ClC1C=CC(=CC=1C(=O)OC)C1C=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-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB321060-5 g
6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol, 95%; .
1261895-50-4 95%
5g
€1159.00 2023-04-26
abcr
AB321060-5g
6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol, 95%; .
1261895-50-4 95%
5g
€1159.00 2025-04-21

Additional information on 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol

Comprehensive Overview of 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261895-50-4)

6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261895-50-4) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research due to its unique structural properties. This compound, often referred to in scientific literature by its CAS number 1261895-50-4, features a chloro-substituted phenyl ring and a methoxycarbonyl group, which contribute to its reactivity and potential applications. Researchers are particularly interested in its role as an intermediate in the synthesis of bioactive molecules, including drug candidates and crop protection agents.

The molecular structure of 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol includes a phenolic hydroxyl group and an aldehyde functionality, making it a versatile building block for further chemical modifications. Its CAS registry number 1261895-50-4 ensures precise identification in global chemical databases, which is critical for regulatory compliance and patent filings. Recent studies highlight its potential in medicinal chemistry, where it serves as a precursor for anti-inflammatory and antimicrobial compounds, aligning with the growing demand for novel therapeutics.

In the context of green chemistry and sustainable synthesis, 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol has been explored for its efficiency in catalyzed reactions and low-waste production methods. These advancements resonate with industry trends toward environmentally friendly processes, a topic frequently searched by professionals in chemical manufacturing and academic research. Additionally, its stability under various conditions makes it a candidate for high-throughput screening in drug discovery pipelines.

Another area of interest is the compound’s potential role in material science, particularly in the development of advanced polymers and functional coatings. The formyl group in its structure allows for cross-linking reactions, which are essential for creating durable materials with tailored properties. This aligns with searches related to smart materials and nanotechnology applications, which are currently trending in scientific communities.

From a commercial perspective, 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol (CAS No. 1261895-50-4) is available through specialized chemical suppliers with certifications for research-grade purity. Its pricing and availability are often queried in procurement databases, reflecting its niche but critical demand. Analytical techniques such as HPLC, NMR, and mass spectrometry are routinely employed to verify its quality, ensuring compliance with Good Laboratory Practice (GLP) standards.

In summary, 6-(4-Chloro-3-methoxycarbonylphenyl)-2-formylphenol represents a multifaceted compound with applications spanning pharmaceuticals, agrochemicals, and materials science. Its CAS number 1261895-50-4 serves as a key identifier for researchers and industry professionals seeking reliable data. As innovation in organic synthesis and sustainable chemistry continues to evolve, this compound is poised to play a pivotal role in addressing contemporary scientific challenges.

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