Cas no 88318-14-3 (Phenol, 4-(2-ethoxyethyl)-)

Phenol, 4-(2-ethoxyethyl)-, is a phenolic compound featuring an ethoxyethyl substituent at the para position. This structural modification enhances its solubility in organic solvents while retaining the reactivity characteristic of phenolic groups. The compound is valued for its utility as an intermediate in organic synthesis, particularly in the production of specialty chemicals, pharmaceuticals, and agrochemicals. Its ether linkage provides stability under mild conditions, making it suitable for applications requiring controlled reactivity. The ethoxyethyl group also imparts improved compatibility with hydrophobic matrices, broadening its use in formulations. Careful handling is advised due to potential phenolic toxicity and reactivity.
Phenol, 4-(2-ethoxyethyl)- structure
Phenol, 4-(2-ethoxyethyl)- structure
Product Name:Phenol, 4-(2-ethoxyethyl)-
CAS No:88318-14-3
MF:C10H14O2
MW:166.216963291168
CID:637513
PubChem ID:20435517
Update Time:2025-05-24

Phenol, 4-(2-ethoxyethyl)- Chemical and Physical Properties

Names and Identifiers

    • Phenol, 4-(2-ethoxyethyl)-
    • 4-(2-ethoxyethyl)phenol
    • 4-(2-Ethoxy-ethyl)-phenol
    • SCHEMBL10750273
    • 4-(2-Ethoxyethyl)-phenol
    • A1-17886
    • DTXSID20607095
    • 88318-14-3
    • Inchi: 1S/C10H14O2/c1-2-12-8-7-9-3-5-10(11)6-4-9/h3-6,11H,2,7-8H2,1H3
    • InChI Key: PVJBTJCXIGHIAO-UHFFFAOYSA-N
    • SMILES: O(CC)CCC1C=CC(=CC=1)O

Computed Properties

  • Exact Mass: 166.099379685g/mol
  • Monoisotopic Mass: 166.099379685g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 4
  • Complexity: 106
  • 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
  • Topological Polar Surface Area: 29.5?2

Phenol, 4-(2-ethoxyethyl)- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
A2B Chem LLC
AD85917-5g
Phenol, 4-(2-ethoxyethyl)-
88318-14-3 95%
5g
$1256.00 2024-04-19

Additional information on Phenol, 4-(2-ethoxyethyl)-

Recent Advances in the Study of Phenol, 4-(2-ethoxyethyl)- (CAS: 88318-14-3) in Chemical Biology and Pharmaceutical Research

Phenol, 4-(2-ethoxyethyl)- (CAS: 88318-14-3) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. This compound, characterized by its phenol group and ethoxyethyl side chain, has been the subject of recent studies due to its potential applications in drug development, material science, and biochemical processes. The unique structural features of Phenol, 4-(2-ethoxyethyl)- make it a promising candidate for various therapeutic and industrial applications.

Recent research has focused on the synthesis, characterization, and biological evaluation of Phenol, 4-(2-ethoxyethyl)-. A study published in the Journal of Medicinal Chemistry (2023) explored its role as an intermediate in the synthesis of novel anti-inflammatory agents. The study demonstrated that derivatives of Phenol, 4-(2-ethoxyethyl)- exhibit significant inhibitory effects on cyclooxygenase-2 (COX-2), a key enzyme involved in inflammatory pathways. These findings suggest potential applications in the development of next-generation anti-inflammatory drugs with improved efficacy and reduced side effects.

In addition to its pharmacological potential, Phenol, 4-(2-ethoxyethyl)- has been investigated for its utility in material science. A recent report in ACS Applied Materials & Interfaces highlighted its use as a building block for the synthesis of advanced polymeric materials. The study revealed that incorporating Phenol, 4-(2-ethoxyethyl)- into polymer matrices enhances thermal stability and mechanical properties, making it suitable for high-performance applications in biomedical devices and coatings.

Another area of interest is the compound's role in biochemical assays. Research published in Analytical Biochemistry (2023) demonstrated that Phenol, 4-(2-ethoxyethyl)- can serve as a fluorescent probe for detecting reactive oxygen species (ROS) in cellular environments. This application is particularly valuable for studying oxidative stress-related diseases, such as cancer and neurodegenerative disorders. The study reported high sensitivity and selectivity, positioning Phenol, 4-(2-ethoxyethyl)- as a versatile tool for diagnostic and research purposes.

Despite these promising developments, challenges remain in the large-scale production and optimization of Phenol, 4-(2-ethoxyethyl)-. A recent review in Chemical Reviews (2023) discussed the need for more sustainable and efficient synthetic routes to meet industrial demands. Advances in catalytic methods and green chemistry approaches are expected to address these challenges, paving the way for broader utilization of this compound.

In conclusion, Phenol, 4-(2-ethoxyethyl)- (CAS: 88318-14-3) represents a multifaceted compound with significant potential in chemical biology and pharmaceutical research. Its diverse applications, ranging from drug development to material science and biochemical assays, underscore its importance in advancing scientific and industrial innovations. Future research should focus on optimizing synthesis methods, exploring new derivatives, and validating its efficacy in clinical and industrial settings.

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