Cas no 56526-87-5 (Phenol, 3-methoxy-2,5-dimethyl-)

Phenol, 3-methoxy-2,5-dimethyl- structure
56526-87-5 structure
Product Name:Phenol, 3-methoxy-2,5-dimethyl-
CAS No:56526-87-5
MF:C9H12O2
MW:152.190382957458
CID:348588
PubChem ID:59796484
Update Time:2025-04-26

Phenol, 3-methoxy-2,5-dimethyl- Chemical and Physical Properties

Names and Identifiers

    • Phenol, 3-methoxy-2,5-dimethyl-
    • 3-methoxy-2,5-dimethylphenol
    • 2,5-dimethyl-3-methoxyphenol
    • EN300-363212
    • DTXSID40732979
    • SCHEMBL10053940
    • 56526-87-5
    • Inchi: 1S/C9H12O2/c1-6-4-8(10)7(2)9(5-6)11-3/h4-5,10H,1-3H3
    • InChI Key: BKTWCYQXHSDAKV-UHFFFAOYSA-N
    • SMILES: O(C)C1C=C(C)C=C(C=1C)O

Computed Properties

  • Exact Mass: 152.08376
  • Monoisotopic Mass: 152.083729621g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 125
  • 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: 2.3
  • Topological Polar Surface Area: 29.5?2

Experimental Properties

  • PSA: 29.46

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Additional information on Phenol, 3-methoxy-2,5-dimethyl-

Introduction to Phenol, 3-methoxy-2,5-dimethyl- (CAS No. 56526-87-5)

Phenol, 3-methoxy-2,5-dimethyl- (CAS No. 56526-87-5) is a versatile organic compound that has garnered significant attention in the fields of chemistry, biology, and pharmaceutical research. This compound, also known as 3-methoxy-2,5-dimethylphenol, is characterized by its unique structural features and diverse applications. In this comprehensive introduction, we will delve into the chemical properties, synthesis methods, biological activities, and potential applications of this compound.

The molecular formula of 3-methoxy-2,5-dimethylphenol is C9H12O2, and its molecular weight is approximately 152.19 g/mol. The compound consists of a phenolic ring with a methoxy group at the 3-position and two methyl groups at the 2- and 5-positions. This specific arrangement of functional groups imparts unique chemical and physical properties to the molecule.

In terms of physical properties, 3-methoxy-2,5-dimethylphenol is a solid at room temperature with a melting point ranging from 70 to 74°C. It is slightly soluble in water but highly soluble in organic solvents such as ethanol and acetone. The compound exhibits moderate stability under standard laboratory conditions but can be sensitive to strong acids and bases.

The synthesis of 3-methoxy-2,5-dimethylphenol can be achieved through various routes. One common method involves the methylation of 3-methoxyphenol using a suitable alkylating agent followed by further functionalization to introduce the additional methyl groups. Another approach involves the selective substitution of a precursor molecule such as 3-methoxybenzene with appropriate reagents to achieve the desired structure. Recent advancements in green chemistry have led to the development of more environmentally friendly synthesis methods that minimize waste and reduce energy consumption.

3-methoxy-2,5-dimethylphenol has been extensively studied for its biological activities. One of its notable properties is its antioxidant activity. Research has shown that this compound can effectively scavenge free radicals and protect cells from oxidative damage. This property makes it a potential candidate for use in cosmetic formulations and dietary supplements aimed at promoting skin health and reducing the signs of aging.

In addition to its antioxidant properties, 3-methoxy-2,5-dimethylphenol has demonstrated anti-inflammatory effects in various biological models. Studies have indicated that it can inhibit the production of pro-inflammatory cytokines such as TNF-α and IL-6, which are key mediators of inflammation. These findings suggest that the compound may have therapeutic potential in treating inflammatory diseases such as arthritis and inflammatory bowel disease.

The antimicrobial activity of 3-methoxy-2,5-dimethylphenol has also been investigated. Research has shown that it exhibits broad-spectrum antimicrobial activity against both Gram-positive and Gram-negative bacteria, as well as certain fungi. This property makes it a promising candidate for use in developing new antimicrobial agents to combat drug-resistant pathogens.

In the pharmaceutical industry, 3-methoxy-2,5-dimethylphenol has been explored as a lead compound for drug discovery. Its unique structure and biological activities make it an attractive starting point for the development of novel therapeutic agents. Ongoing research is focused on optimizing its pharmacological properties through structural modifications and evaluating its efficacy in preclinical models.

Beyond its applications in healthcare and pharmaceuticals, 3-methoxy-2,5-dimethylphenol has found use in other industries such as agriculture and materials science. In agriculture, it has been studied for its potential as a natural pesticide due to its antimicrobial properties. In materials science, it has been used as a building block for synthesizing advanced materials with tailored properties.

The environmental impact of 3-methoxy-2,5-dimethylphenol is an important consideration in its industrial applications. Studies have shown that it can be biodegraded by certain microorganisms under aerobic conditions, which suggests that it may have a lower environmental impact compared to some other synthetic compounds. However, further research is needed to fully understand its long-term effects on ecosystems.

In conclusion, Phenol, 3-methoxy-2,5-dimethyl- (CAS No. 56526-87-5) is a multifaceted compound with a wide range of applications across various fields. Its unique chemical structure endows it with valuable properties such as antioxidant activity, anti-inflammatory effects, and antimicrobial activity. Ongoing research continues to uncover new potential uses for this compound, making it an exciting area of study for scientists and researchers worldwide.

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