Cas no 179178-90-6 ([3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid)

[3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid is a versatile organic compound featuring both phenylacetic acid and methoxycarbonylmethyl functional groups. Its bifunctional structure makes it valuable as an intermediate in pharmaceutical and fine chemical synthesis, particularly in the preparation of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. The presence of the methoxycarbonylmethyl group enhances reactivity in esterification and coupling reactions, while the phenylacetic acid moiety provides a stable aromatic backbone. This compound is characterized by high purity and consistent performance, ensuring reliable results in research and industrial applications. Its well-defined structure facilitates precise modifications, making it a preferred choice for synthetic chemists.
[3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid structure
179178-90-6 structure
Product Name:[3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid
CAS No:179178-90-6
MF:C11H12O4
MW:208.210583686829
MDL:MFCD11846355
CID:2138051
PubChem ID:21700134
Update Time:2025-11-02

[3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid Chemical and Physical Properties

Names and Identifiers

    • [3-(2-methoxy-2-oxoethyl)phenyl]acetic acid
    • CVSJWBIWUPDLBV-UHFFFAOYSA-N
    • 1,3-phenylenediacetic acid methyl ester
    • [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid
    • MDL: MFCD11846355
    • Inchi: 1S/C11H12O4/c1-15-11(14)7-9-4-2-3-8(5-9)6-10(12)13/h2-5H,6-7H2,1H3,(H,12,13)
    • InChI Key: CVSJWBIWUPDLBV-UHFFFAOYSA-N
    • SMILES: O(C)C(CC1C=CC=C(CC(=O)O)C=1)=O

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 5
  • Complexity: 237
  • XLogP3: 1.3
  • Topological Polar Surface Area: 63.6

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Additional information on [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid

Comprehensive Guide to [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid (CAS No. 179178-90-6): Properties, Applications, and Market Insights

[3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid (CAS No. 179178-90-6) is a specialized organic compound with significant relevance in pharmaceutical and chemical research. This phenylacetic acid derivative is characterized by its unique molecular structure, featuring a methoxy-oxoethyl side chain that enhances its reactivity and functionality. The compound's CAS number 179178-90-6 serves as a critical identifier in chemical databases, ensuring precise tracking in research and industrial applications.

The growing interest in phenylacetic acid derivatives like [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid is driven by their versatility in drug development. Researchers frequently search for "CAS 179178-90-6 applications" or "synthesis of 3-(2-Methoxy-2-oxoethyl)phenyl acetic acid," reflecting its importance in medicinal chemistry. This compound is particularly valued for its potential as an intermediate in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other therapeutic agents.

From a chemical perspective, [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid exhibits notable stability under standard conditions, making it suitable for various synthetic processes. Its methoxy-oxoethyl group contributes to enhanced solubility in organic solvents, a property frequently explored in "solubility of phenylacetic acid derivatives" searches. The compound's molecular weight of 208.21 g/mol and precise structural configuration are often discussed in academic papers and patent literature.

The pharmaceutical industry shows increasing demand for CAS 179178-90-6, particularly in the development of targeted drug delivery systems. Recent trends in "green chemistry approaches for phenylacetic acid synthesis" highlight the compound's compatibility with environmentally friendly production methods. This aligns with global sustainability initiatives while maintaining the high purity standards required for pharmaceutical intermediates.

Analytical techniques for [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid characterization include HPLC, NMR spectroscopy, and mass spectrometry. These methods address common queries like "how to analyze phenylacetic acid derivatives" and ensure quality control in industrial settings. The compound's distinct spectral signatures facilitate its identification in complex mixtures, making it valuable for analytical method development.

Market analysis reveals steady growth in the phenylacetic acid derivatives market, with CAS 179178-90-6 occupying a niche segment. Pharmaceutical companies increasingly search for "reliable suppliers of 3-(2-Methoxy-2-oxoethyl)phenyl acetic acid" as they expand their API manufacturing capabilities. The compound's pricing trends reflect its specialized nature and the technical expertise required for its production.

In research applications, [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid serves as a building block for more complex molecules. Its structural features enable modifications that address current challenges in "drug bioavailability improvement" and "metabolic stability enhancement." These applications contribute to its prominence in scientific literature and patent filings.

Storage and handling recommendations for CAS 179178-90-6 emphasize standard laboratory precautions, with particular attention to moisture control. This information responds to frequent searches about "stability of phenylacetic acid derivatives" and ensures proper material management throughout the supply chain.

The future outlook for [3-(2-Methoxy-2-oxoethyl)phenyl]acetic acid appears promising, with potential expansions into new therapeutic areas. Emerging research into "multi-functional pharmaceutical intermediates" positions this compound as a valuable asset in drug discovery pipelines. Continued innovation in synthetic methodologies will likely enhance its accessibility and application scope.

For researchers and industry professionals, understanding the full potential of CAS 179178-90-6 requires staying updated with the latest publications and market trends. The compound's unique properties ensure its ongoing relevance in both academic and industrial chemistry sectors, making it a subject of continuous scientific and commercial interest.

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