Cas no 78055-65-9 (Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester)

Phosphonic acid, P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester is an organophosphorus compound featuring a phosphonate ester group linked to a 3,4-dimethoxybenzyl moiety. This structure imparts stability and reactivity, making it useful in organic synthesis, particularly as an intermediate in the preparation of biologically active molecules or functional materials. The diethyl ester group enhances solubility in organic solvents, facilitating its use in cross-coupling reactions or as a precursor for further derivatization. Its aromatic dimethoxy substitution may contribute to electronic modulation in coordination chemistry or agrochemical applications. The compound's well-defined molecular architecture allows for precise incorporation into more complex systems, underscoring its utility in research and industrial processes.
Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester structure
78055-65-9 structure
Product Name:Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester
CAS No:78055-65-9
MF:C13H21O5P
MW:288.276605367661
CID:573381
PubChem ID:157150
Update Time:2025-06-14

Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester Chemical and Physical Properties

Names and Identifiers

    • Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester
    • (3,4-DIMETHOXY-BENZYL)-PHOSPHONIC ACID DIETHYL ESTER
    • 4-(diethoxyphosphorylmethyl)-1,2-dimethoxybenzene
    • AC1L4HH3
    • AC1Q38AS
    • AG-H-13051
    • CTK5E5329
    • diethyl (3,4-dimethoxybenzyl)phosphonate
    • diethyl (3,4-dimethoxyphenyl)methylphosphonate
    • diethyl 3,4-dimethoxybenzylphosphonate
    • Phosphonic acid, ((3,4-dimethoxyphenyl)methyl)-, diethyl ester
    • 78055-65-9
    • AKOS015843620
    • Phosphonic acid, [(3,4-dimethoxyphenyl)methyl]-, diethyl ester
    • SCHEMBL9950354
    • DTXSID40228701
    • 3-BIPHENYL-4-FORMYL-ACETICACID
    • FT-0651319
    • Diethyl3,4-dimethoxybenzylphosphonate
    • MDL: MFCD00433618
    • Inchi: 1S/C13H21O5P/c1-5-17-19(14,18-6-2)10-11-7-8-12(15-3)13(9-11)16-4/h7-9H,5-6,10H2,1-4H3
    • InChI Key: QKPSYROBCCDFGW-UHFFFAOYSA-N
    • SMILES: P(CC1C=CC(=C(C=1)OC)OC)(=O)(OCC)OCC

Computed Properties

  • Exact Mass: 288.11273
  • Monoisotopic Mass: 288.11266076g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 8
  • Complexity: 287
  • 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: 1.3
  • Topological Polar Surface Area: 54?2

Experimental Properties

  • PSA: 53.99

Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester Pricemore >>

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Additional information on Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester

Comprehensive Overview of Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester (CAS No. 78055-65-9)

Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester (CAS No. 78055-65-9) is a specialized organic compound with significant applications in various industries. This compound, often referred to by its systematic name, belongs to the class of phosphonate esters, which are known for their versatility in chemical synthesis and industrial processes. The presence of the 3,4-dimethoxyphenyl group and the diethyl ester moiety makes this compound particularly interesting for researchers and manufacturers alike.

In recent years, the demand for phosphonate-based compounds has surged due to their unique properties, such as stability under harsh conditions and compatibility with other chemicals. Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester is no exception. Its molecular structure allows it to act as an intermediate in the synthesis of more complex molecules, making it a valuable asset in pharmaceuticals, agrochemicals, and material science. Users searching for "phosphonate ester applications" or "CAS 78055-65-9 uses" will find this compound particularly relevant.

One of the most frequently asked questions about Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester revolves around its synthesis and purification. The compound is typically synthesized through a series of esterification and alkylation reactions, starting from readily available precursors. Researchers often inquire about "how to synthesize phosphonate esters" or "optimizing diethyl ester production," highlighting the growing interest in efficient and scalable methods for its preparation.

The 3,4-dimethoxyphenyl group in this compound is a key feature that contributes to its reactivity and functionality. This aromatic moiety is known for its electron-donating properties, which can influence the compound's behavior in catalytic reactions or as a ligand in coordination chemistry. For those exploring "aryl-substituted phosphonates" or "dimethoxyphenyl derivatives," this compound offers a compelling case study.

From an industrial perspective, Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester is often utilized as a building block for more complex molecules. Its ability to undergo further chemical transformations, such as hydrolysis or cross-coupling reactions, makes it a versatile intermediate. Companies and researchers looking for "high-purity phosphonate intermediates" or "custom chemical synthesis" frequently consider this compound for their projects.

Environmental and safety considerations are also paramount when working with phosphonate esters. While Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester is generally stable under normal conditions, proper handling and storage are essential to ensure its longevity and performance. Queries like "phosphonate ester stability" or "safe handling of diethyl esters" reflect the community's focus on sustainable and responsible chemical practices.

In conclusion, Phosphonic acid,P-[(3,4-dimethoxyphenyl)methyl]-, diethyl ester (CAS No. 78055-65-9) is a compound of considerable interest due to its structural features and broad applicability. Whether you are a chemist exploring new synthetic routes, an industrial player seeking reliable intermediates, or a researcher investigating phosphonate chemistry, this compound offers a wealth of opportunities. Its relevance in modern chemistry is underscored by the numerous searches for "phosphonate ester properties" and "CAS 78055-65-9 suppliers," making it a topic worthy of in-depth study.

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