Cas no 90534-24-0 (5-Ethoxy-2-methylphenol)

5-Ethoxy-2-methylphenol is a phenolic compound characterized by its ethoxy and methyl substituents on the aromatic ring. This structure imparts unique chemical properties, making it useful as an intermediate in organic synthesis, particularly in the production of fragrances, pharmaceuticals, and agrochemicals. Its ether and hydroxyl functional groups enhance reactivity in electrophilic aromatic substitution and coupling reactions. The compound exhibits moderate solubility in organic solvents and stability under standard conditions, facilitating handling and storage. Its distinct substitution pattern also allows for selective functionalization, enabling tailored applications in fine chemical manufacturing. Care should be taken to avoid exposure due to potential irritant properties.
5-Ethoxy-2-methylphenol structure
5-Ethoxy-2-methylphenol structure
Product Name:5-Ethoxy-2-methylphenol
CAS No:90534-24-0
MF:C9H12O2
MW:152.190382957458
MDL:MFCD20534917
CID:788649
Update Time:2025-10-15

5-Ethoxy-2-methylphenol Chemical and Physical Properties

Names and Identifiers

    • Phenol, 5-ethoxy-2-methyl-
    • 5-Ethoxy-2-methylphenol
    • MDL: MFCD20534917
    • Inchi: 1S/C9H12O2/c1-3-11-8-5-4-7(2)9(10)6-8/h4-6,10H,3H2,1-2H3
    • InChI Key: ZNRIAYQDHYBINQ-UHFFFAOYSA-N
    • SMILES: O(CC)C1C=CC(C)=C(C=1)O

Computed Properties

  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2

5-Ethoxy-2-methylphenol Pricemore >>

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$ 50.00 2022-06-05
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Additional information on 5-Ethoxy-2-methylphenol

5-Ethoxy-2-methylphenol: A Comprehensive Overview

5-Ethoxy-2-methylphenol (CAS No. 90534-24-0) is a versatile organic compound with a unique chemical structure that has garnered significant attention in various scientific and industrial applications. This compound, also referred to as o-methyl-5-ethoxyphenol, belongs to the class of phenolic compounds, which are known for their diverse functional properties. Its molecular formula is C11H16O3, and it features a phenolic hydroxyl group, an ethoxy substituent, and a methyl group attached to the aromatic ring.

The synthesis of 5-Ethoxy-2-methylphenol typically involves multi-step organic reactions, often utilizing Friedel-Crafts alkylation or acylation techniques followed by hydrolysis or oxidation steps. Recent advancements in catalytic systems have enabled more efficient and environmentally friendly production methods, reducing the overall cost and improving yield rates. Researchers have also explored the use of microwave-assisted synthesis, which has shown promise in accelerating reaction times while maintaining product purity.

One of the most intriguing aspects of 5-Ethoxy-2-methylphenol is its biological activity. Studies have demonstrated that this compound exhibits significant antioxidant properties, making it a potential candidate for applications in the pharmaceutical and cosmetic industries. For instance, its ability to scavenge free radicals has been extensively studied using modern analytical techniques such as electron paramagnetic resonance (EPR) spectroscopy and high-performance liquid chromatography (HPLC). These findings suggest that 5-Ethoxy-2-methylphenol could be used as a natural preservative or anti-aging agent in skincare products.

In addition to its antioxidant properties, 5-Ethoxy-2-methylphenol has shown promising results in anti-inflammatory assays. Preclinical studies using animal models have indicated that this compound can inhibit the production of pro-inflammatory cytokines such as tumor necrosis factor-alpha (TNF-α) and interleukin-6 (IL-6). These findings have sparked interest in exploring its potential as a therapeutic agent for inflammatory diseases such as arthritis and dermatitis.

The environmental impact of 5-Ethoxy-2-methylphenol has also been a topic of recent research. Studies on its biodegradability and toxicity have revealed that it is relatively non-toxic to aquatic organisms at concentrations typically found in industrial effluents. This makes it a safer alternative to some traditional chemicals used in manufacturing processes.

From an industrial perspective, 5-Ethoxy-2-methylphenol finds applications in the synthesis of advanced materials such as polyurethanes and resins. Its ability to act as a reactive diluent or curing agent has been leveraged in the development of high-performance coatings and adhesives. Recent innovations in polymer chemistry have further expanded its utility by incorporating it into biodegradable polymers for sustainable packaging solutions.

In conclusion, 5-Ethoxy-2-methylphenol (CAS No. 90534-24-0) is a multifaceted compound with immense potential across various industries. Its unique chemical properties, coupled with recent advancements in synthesis and application techniques, position it as a key player in the development of innovative products and therapies.

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