Cas no 887412-01-3 (Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]-)

Benzoic acid, 4-[4-(2-methoxyethoxy)phenoxy]-, is a specialized aromatic carboxylic acid derivative featuring a phenoxy ether linkage with a methoxyethoxy side chain. This structural configuration imparts unique solubility and reactivity properties, making it valuable in organic synthesis and pharmaceutical intermediates. The ether and carboxylic acid functionalities enhance its utility as a building block for more complex molecules, particularly in drug development and fine chemical applications. Its balanced polarity allows for compatibility with both aqueous and organic phases, facilitating diverse reaction conditions. The compound’s stability under moderate temperatures further supports its use in controlled synthetic processes.
Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- structure
887412-01-3 structure
Product Name:Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]-
CAS No:887412-01-3
MF:C16H16O5
MW:288.295245170593
MDL:MFCD07779207
CID:713033
Update Time:2026-04-29

Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- Chemical and Physical Properties

Names and Identifiers

    • Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]-
    • 4-[4-(2-methoxyethoxy)phenoxy]benzoic acid
    • 4-[4-(2-METHOXY-ETHOXY)-PHENOXY]-BENZOIC ACID
    • MDL: MFCD07779207

Computed Properties

  • Exact Mass: 288.10000
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 21
  • Rotatable Bond Count: 7
  • Complexity: 304
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 2.8

Experimental Properties

  • PSA: 64.99000
  • LogP: 3.20230

Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- Pricemore >>

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Additional information on Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]-

Comprehensive Overview of Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- (CAS No. 887412-01-3)

Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- (CAS No. 887412-01-3) is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, agrochemicals, and material science. This compound, characterized by its unique molecular structure, combines a benzoic acid core with a phenoxy group and a methoxyethoxy side chain. Such structural features make it a versatile intermediate in synthetic chemistry, particularly in the development of advanced materials and bioactive molecules.

In recent years, the demand for Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- has surged due to its potential applications in drug discovery and green chemistry. Researchers are increasingly exploring its role as a building block for biodegradable polymers and sustainable coatings, aligning with global trends toward environmental sustainability. Its compatibility with photoactive materials also makes it a candidate for use in organic electronics, such as OLEDs and solar cells, addressing the growing need for renewable energy solutions.

The synthesis of Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- typically involves multi-step organic reactions, including etherification and esterification processes. Advanced techniques like microwave-assisted synthesis and catalytic hydrogenation have been employed to enhance yield and purity, reflecting the compound's relevance in modern process optimization strategies. Analytical methods such as HPLC and NMR spectroscopy are critical for quality control, ensuring compliance with industry standards.

From a commercial perspective, Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- is often sought after by manufacturers of specialty chemicals and pharmaceutical intermediates. Its stability under various conditions and solubility in common organic solvents like DMSO and ethanol further enhance its utility. Market analysts note its rising prominence in Asia-Pacific regions, driven by expanding R&D investments in fine chemicals.

Safety and regulatory aspects of Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- are equally important. While it is not classified as hazardous under current guidelines, proper handling protocols—including the use of personal protective equipment (PPE)—are recommended during laboratory-scale operations. Regulatory bodies such as the EPA and REACH have reviewed its environmental impact, confirming its low toxicity profile when disposed of responsibly.

Looking ahead, the compound's potential in nanotechnology and biomedical engineering is under active investigation. For instance, its derivatization could lead to novel drug delivery systems or bioimaging agents, topics frequently searched by academic and industrial researchers. As the scientific community continues to explore its applications, Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- remains a compelling subject for innovation.

In summary, Benzoic acid,4-[4-(2-methoxyethoxy)phenoxy]- (CAS No. 887412-01-3) exemplifies the intersection of chemistry and cutting-edge technology. Its adaptability across multiple industries, coupled with its alignment with sustainability goals, positions it as a compound of enduring relevance. For those seeking detailed technical data or procurement options, reputable suppliers often provide COA (Certificate of Analysis) and MSDS documentation to ensure transparency and compliance.

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