Cas no 26691-28-1 (2-(4-ethoxy-3-hydroxyphenyl)acetic acid)

2-(4-Ethoxy-3-hydroxyphenyl)acetic acid is a phenolic derivative with a molecular structure featuring both ethoxy and hydroxyl functional groups on the aromatic ring, along with an acetic acid side chain. This compound is of interest in organic synthesis and pharmaceutical research due to its versatile reactivity, particularly in the formation of esters, amides, or other derivatives. The presence of the hydroxyl group enhances its potential as an intermediate in the synthesis of bioactive molecules, while the ethoxy group contributes to its solubility and stability. Its well-defined structure makes it suitable for applications in medicinal chemistry, where precise functionalization is required.
2-(4-ethoxy-3-hydroxyphenyl)acetic acid structure
26691-28-1 structure
Product Name:2-(4-ethoxy-3-hydroxyphenyl)acetic acid
CAS No:26691-28-1
MF:C10H12O4
MW:196.199883460999
MDL:MFCD00016830
CID:3166450
PubChem ID:21819849
Update Time:2025-06-29

2-(4-ethoxy-3-hydroxyphenyl)acetic acid Chemical and Physical Properties

Names and Identifiers

    • 4-Ethoxy-3-hydroxyphenylacetic Acid
    • 2-(4-ETHOXY-3-HYDROXYPHENYL)ACETIC ACID
    • Benzeneacetic acid, 4-ethoxy-3-hydroxy-
    • AKOS027460850
    • SCHEMBL6036311
    • 26691-28-1
    • AC5769
    • CS-0450349
    • MFCD00016830
    • 2-(4-ethoxy-3-hydroxyphenyl)aceticacid
    • SY039208
    • 2-(4-ethoxy-3-hydroxyphenyl)acetic acid
    • MDL: MFCD00016830
    • Inchi: 1S/C10H12O4/c1-2-14-9-4-3-7(5-8(9)11)6-10(12)13/h3-5,11H,2,6H2,1H3,(H,12,13)
    • InChI Key: KBJNAVBOVXYTOH-UHFFFAOYSA-N
    • SMILES: C1(CC(O)=O)=CC=C(OCC)C(O)=C1

Computed Properties

  • Exact Mass: 196.07355886Da
  • Monoisotopic Mass: 196.07355886Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 193
  • 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: 66.8?2

Experimental Properties

  • Color/Form: No data available
  • Density: 1.3±0.1 g/cm3
  • Melting Point: No data available
  • Boiling Point: 378.8±27.0 °C at 760 mmHg
  • Flash Point: 152.1±17.2 °C
  • Vapor Pressure: 0.0±0.9 mmHg at 25°C

2-(4-ethoxy-3-hydroxyphenyl)acetic acid Pricemore >>

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Additional information on 2-(4-ethoxy-3-hydroxyphenyl)acetic acid

2-(4-Ethoxy-3-Hydroxyphenyl)Acetic Acid: A Comprehensive Overview

2-(4-Ethoxy-3-Hydroxyphenyl)Acetic Acid, also known by its CAS number CAS No 26691-28-1, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound has been extensively studied for its potential applications in drug development, particularly in the context of its bioactivity and structural properties. Recent advancements in analytical techniques and computational modeling have further elucidated its mechanisms of action and therapeutic potential.

The molecular structure of 2-(4-Ethoxy-3-Hydroxyphenyl)Acetic Acid comprises a phenyl ring substituted with ethoxy and hydroxyl groups, along with an acetic acid moiety. This unique arrangement contributes to its ability to interact with various biological targets, including enzymes and receptors. Researchers have highlighted the importance of the hydroxyl group in facilitating hydrogen bonding, which plays a crucial role in its pharmacokinetic properties.

Recent studies have focused on the synthesis and characterization of CAS No 26691-28-1. Advanced synthetic methodologies, such as Suzuki coupling and Stille coupling, have been employed to optimize the production process. These methods not only enhance yield but also improve the purity of the compound, which is critical for its use in preclinical studies.

The pharmacological activity of 2-(4-Ethoxy-3-Hydroxyphenyl)Acetic Acid has been extensively investigated. In vitro assays have demonstrated its potential as an anti-inflammatory agent, with studies indicating its ability to inhibit cyclooxygenase enzymes. Additionally, research into its anti-cancer properties has revealed that it may induce apoptosis in certain cancer cell lines, suggesting a promising avenue for oncology applications.

In terms of bioavailability, recent pharmacokinetic studies have provided valuable insights into the absorption, distribution, metabolism, and excretion (ADME) profile of CAS No 26691-28-1. These studies have highlighted the importance of formulation strategies to enhance its stability and bioavailability, which are critical factors for successful drug delivery.

The application of computational chemistry tools has further enriched our understanding of this compound. Molecular docking studies have provided insights into its binding affinities with various protein targets, while quantum mechanical calculations have shed light on its electronic properties and reactivity.

In conclusion, 2-(4-Ethoxy-3-Hydroxyphenyl)Acetic Acid (CAS No 26691-28-1) represents a promising candidate for drug development due to its diverse pharmacological activities and favorable chemical properties. Continued research into its synthesis, characterization, and therapeutic applications will undoubtedly contribute to the advancement of medicinal chemistry.

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