Cas no 71360-04-8 (Phosphine oxide, bis(2-methoxyphenyl)-)

Phosphine oxide, bis(2-methoxyphenyl)-, is an organophosphorus compound characterized by its two 2-methoxyphenyl substituents bonded to a central phosphorus oxide group. This structure imparts stability and moderate polarity, making it useful as a ligand in coordination chemistry and as an intermediate in organic synthesis. Its electron-withdrawing properties enhance reactivity in cross-coupling reactions, while the methoxy groups contribute to solubility in organic solvents. The compound is also studied for potential applications in materials science, particularly in the development of flame retardants and photoactive materials. Its well-defined molecular architecture ensures consistent performance in specialized chemical processes.
Phosphine oxide, bis(2-methoxyphenyl)- structure
71360-04-8 structure
Product Name:Phosphine oxide, bis(2-methoxyphenyl)-
CAS No:71360-04-8
MF:C14H14O3P
MW:261.232924938202
MDL:MFCD33022345
CID:2799933
PubChem ID:11196297
Update Time:2025-05-20

Phosphine oxide, bis(2-methoxyphenyl)- Chemical and Physical Properties

Names and Identifiers

    • bis(2-methoxyphenyl)-oxophosphanium
    • DTXSID20458428
    • CS-0160256
    • 1-methoxy-2-[(2-methoxyphenyl)phosphoroso]benzene
    • BIS(2-METHOXYPHENYL)(OXO)-??-PHOSPHANYLIUM
    • E74541
    • Bis(2-methoxyphenyl)phosphineoxide
    • DB-400722
    • 1-methoxy-2-(2-methoxyphenylphosphoroso)benzene
    • Phosphine oxide, bis(2-methoxyphenyl)-
    • MWYXORYWUKRJEX-UHFFFAOYSA-N
    • 1-methoxy-2-(2-methoxyphenyl)phosphonoyl-benzene
    • AKOS040768502
    • 71360-04-8
    • Bis(2-methoxyphenyl)phosphine oxide
    • SCHEMBL2153848
    • MDL: MFCD33022345
    • Inchi: 1S/C14H14O3P/c1-16-11-7-3-5-9-13(11)18(15)14-10-6-4-8-12(14)17-2/h3-10H,1-2H3/q+1
    • InChI Key: MWYXORYWUKRJEX-UHFFFAOYSA-N
    • SMILES: [P+](C1C=CC=CC=1OC)(C1C=CC=CC=1OC)=O

Computed Properties

  • Exact Mass: 261.06805630g/mol
  • Monoisotopic Mass: 261.06805630g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 4
  • Complexity: 256
  • 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: 2.4
  • Topological Polar Surface Area: 35.5?2

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Phosphine oxide, bis(2-methoxyphenyl)- Suppliers

Suzhou Senfeida Chemical Co., Ltd
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(CAS:71360-04-8)bis(2-methoxyphenyl)-oxophosphanium
Order Number:sfd5384
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:33
Price ($):discuss personally

Additional information on Phosphine oxide, bis(2-methoxyphenyl)-

Phosphine oxide, bis(2-methoxyphenyl)- (CAS No. 71360-04-8): A Comprehensive Overview

Phosphine oxide, bis(2-methoxyphenyl)-, identified by its CAS number 71360-04-8, is a significant compound in the realm of organic chemistry and has garnered considerable attention due to its unique structural and functional properties. This compound, characterized by its bidentate phosphine oxide moiety linked to two 2-methoxyphenyl groups, exhibits a range of applications that span from catalysis to pharmaceutical intermediates. The detailed exploration of this molecule not only highlights its chemical significance but also integrates the latest research findings to provide a comprehensive understanding of its potential and utility.

The molecular structure of Phosphine oxide, bis(2-methoxyphenyl)- consists of a central phosphorus atom coordinated to two oxygen atoms, forming a phosphine oxide ligand. This ligand is further substituted with two 2-methoxyphenyl groups, which contribute to the compound's overall steric and electronic environment. The presence of the methoxy groups enhances the compound's solubility in polar solvents and influences its reactivity in various chemical transformations.

In recent years, Phosphine oxide, bis(2-methoxyphenyl)- has been extensively studied for its role as a ligand in transition metal catalysis. The bidentate nature of the phosphine oxide moiety allows it to form stable complexes with various transition metals, such as palladium, platinum, and nickel. These metal complexes have been employed in a multitude of catalytic processes, including cross-coupling reactions, hydrogenation reactions, and oxidation reactions. The latest research has demonstrated that the use of Phosphine oxide, bis(2-methoxyphenyl)- as a ligand can significantly enhance the efficiency and selectivity of these catalytic processes.

One notable application of Phosphine oxide, bis(2-methoxyphenyl)- is in the synthesis of complex organic molecules. Its ability to stabilize reactive intermediates and facilitate multiple bond formations makes it an invaluable tool in synthetic organic chemistry. For instance, recent studies have shown that this compound can be used to catalyze the formation of carbon-carbon bonds in the synthesis of pharmaceutical intermediates. The precision and efficiency offered by these catalytic systems have opened new avenues for the development of novel therapeutic agents.

The pharmaceutical industry has also shown interest in Phosphine oxide, bis(2-methoxyphenyl)- due to its potential as an intermediate in drug synthesis. The compound's structural features allow it to participate in various chemical reactions that are crucial for the formation of biologically active molecules. Researchers have been exploring its utility in the synthesis of kinase inhibitors, which are widely used in the treatment of cancer and inflammatory diseases. The ability of this compound to modulate enzyme activity has made it a promising candidate for further development into therapeutic agents.

In addition to its applications in catalysis and pharmaceuticals, Phosphine oxide, bis(2-methoxyphenyl)- has found utility in materials science. Its unique electronic properties make it suitable for use in organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Recent advancements in this field have demonstrated that incorporating this compound into these devices can improve their performance by enhancing charge transport properties.

The environmental impact of using Phosphine oxide, bis(2-methoxyphenyl)- has also been a subject of research. Studies have shown that this compound is biodegradable under certain conditions, which makes it an environmentally friendly alternative to other phosphine-based ligands. This characteristic is particularly important in industrial applications where waste management and sustainability are key concerns.

The synthesis of Phosphine oxide, bis(2-methoxyphenyl)- involves multi-step organic reactions that require careful optimization to ensure high yield and purity. Recent improvements in synthetic methodologies have enabled more efficient production processes, making this compound more accessible for research and industrial applications. These advancements include the use of greener solvents and catalysts, which reduce the environmental footprint of the synthesis process.

The future prospects for Phosphine oxide, bis(2-methoxyphenyl)- are promising, with ongoing research aimed at expanding its applications and understanding its fundamental properties. As our knowledge of molecular interactions continues to grow, it is expected that new uses for this compound will emerge across various scientific disciplines. The integration of computational chemistry and advanced spectroscopic techniques will further enhance our ability to study its behavior and optimize its applications.

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Suzhou Senfeida Chemical Co., Ltd
(CAS:71360-04-8)bis(2-methoxyphenyl)-oxophosphanium
sfd5384
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
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