Cas no 926204-10-6 ([1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY)

1,1'-Biphenyl]-3-carboxaldehyde,6-ethoxy-5-methoxy is a biphenyl-based aldehyde derivative featuring ethoxy and methoxy substituents at the 6- and 5-positions, respectively. This compound is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The presence of both alkoxy groups enhances its reactivity in electrophilic aromatic substitution and cross-coupling reactions, while the aldehyde functionality allows for further derivatization. Its well-defined structure and consistent purity make it suitable for applications requiring precise molecular frameworks. The compound is typically handled under controlled conditions due to its sensitivity to oxidation and light.
[1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY structure
926204-10-6 structure
Product Name:[1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY
CAS No:926204-10-6
MF:C16H16O3
MW:256.296444892883
CID:1974132
Update Time:2025-10-28

[1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY Chemical and Physical Properties

Names and Identifiers

    • [1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY
    • 4-ethoxy-3-methoxy-5-phenylbenzaldehyde
    • Inchi： 1S/C16H16O3/c1-3-19-16-14(13-7-5-4-6-8-13)9-12(11-17)10-15(16)18-2/h4-11H,3H2,1-2H3
    • InChI Key： HXYSQYUOBVXTSV-UHFFFAOYSA-N
    • SMILES： C1(C2=CC=CC=C2)=C(OCC)C(OC)=CC(C=O)=C1

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 5

[1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1559419-1g
6-Ethoxy-5-methoxy-[1,1'-biphenyl]-3-carbaldehyde
 926204-10-6 98%
1g
 ￥10392.00 2024-04-25

[1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY Related Literature

Additional information on [1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY

Comprehensive Overview of [1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY (CAS No. 926204-10-6)

The compound [1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY (CAS No. 926204-10-6) is a specialized organic molecule with significant applications in pharmaceutical research, agrochemical development, and material science. Its unique structure, featuring a biphenyl core substituted with ethoxy and methoxy groups, makes it a valuable intermediate in synthetic chemistry. Researchers and industries are increasingly interested in this compound due to its potential in designing novel drugs, fragrances, and advanced materials.

One of the most searched questions related to [1,1'-BIPHENYL]-3-CARBOXALDEHYDE is its role in drug discovery. Recent studies highlight its utility as a building block for heterocyclic compounds, which are pivotal in developing anti-inflammatory and antioxidant agents. The presence of the aldehyde functional group allows for versatile chemical transformations, enabling the creation of derivatives with tailored biological activities. This aligns with the growing demand for small-molecule therapeutics in the pharmaceutical industry.

Another hot topic is the compound's application in green chemistry. With sustainability becoming a global priority, researchers are exploring eco-friendly synthesis routes for 6-ETHOXY-5-METHOXY derivatives. Innovations such as catalytic oxidation and solvent-free reactions are being tested to reduce environmental impact. These advancements resonate with the increasing searches for sustainable chemical processes and biodegradable intermediates.

In material science, [1,1'-BIPHENYL]-3-CARBOXALDEHYDE is gaining attention for its potential in organic electronics. Its conjugated system and electron-rich substituents make it a candidate for OLEDs (Organic Light-Emitting Diodes) and photovoltaic cells. As the demand for flexible displays and renewable energy solutions surges, this compound's role in optoelectronic materials is being actively investigated.

The compound's CAS No. 926204-10-6 is frequently queried in databases like SciFinder and PubChem, reflecting its relevance in academic and industrial research. Analytical techniques such as NMR spectroscopy and mass spectrometry are commonly used to characterize its purity and structure, addressing another common search trend: analytical methods for biphenyl derivatives.

Safety and handling of [1,1'-BIPHENYL]-3-CARBOXALDEHYDE are also trending topics. While not classified as hazardous, proper storage conditions (e.g., cool, dry environments) and personal protective equipment (PPE) are recommended. This aligns with the broader search interest in chemical safety protocols and lab best practices.

In summary, [1,1'-BIPHENYL]-3-CARBOXALDEHYDE,6-ETHOXY-5-METHOXY (CAS No. 926204-10-6) is a multifaceted compound with expanding applications in life sciences and advanced materials. Its integration into cutting-edge research and alignment with sustainability goals ensure its continued relevance in the scientific community.

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