Cas no 4317-61-7 (1-(2-Methylphenoxy)-2-propanol)

1-(2-Methylphenoxy)-2-propanol is a phenolic ether alcohol with applications in organic synthesis and industrial chemistry. Its structure combines a 2-methylphenoxy group with a propanol moiety, offering reactivity suitable for use as an intermediate in the production of specialty chemicals. The compound exhibits moderate polarity, enhancing its solubility in both organic solvents and partially aqueous systems, which can be advantageous in formulation processes. Its stability under standard conditions and compatibility with various reagents make it a versatile building block for synthesizing more complex molecules. The presence of the methyl group on the aromatic ring may influence its reactivity in electrophilic substitution reactions, providing selectivity in synthetic pathways.
1-(2-Methylphenoxy)-2-propanol structure
4317-61-7 structure
Product Name:1-(2-Methylphenoxy)-2-propanol
CAS No:4317-61-7
MF:C10H14O2
MW:166.216963291168
MDL:MFCD00191542
CID:330906
PubChem ID:87573032
Update Time:2025-10-29

1-(2-Methylphenoxy)-2-propanol Chemical and Physical Properties

Names and Identifiers

    • 2-Propanol,1-(2-methylphenoxy)-
    • 1-(2-Methylphenoxy)-2-propanol
    • 1-(2-methylphenoxy)propan-2-ol
    • 1-(o-Tolyloxy)-2-propanol
    • 1-(o-Tolyloxy)propan-2-ol
    • 2-Propanol, 1-(o-tolyloxy)-
    • 1-(2-Methylphenoxy)-2-propanol, AldrichCPR
    • o-Cresoxy-2-propanol
    • Propanol, 1(or 2)-phenoxy-
    • 3-(2-methylphenoxy) propan-2-ol
    • M1063
    • MDL: MFCD00191542
    • Inchi: 1S/C10H14O2/c1-8-5-3-4-6-10(8)12-7-9(2)11/h3-6,9,11H,7H2,1-2H3
    • InChI Key: ISIQEWJJVXFCDP-UHFFFAOYSA-N
    • SMILES: O(C1C=CC=CC=1C)CC(C)O
    • BRN: 2963088

Computed Properties

  • Exact Mass: 166.09900
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 125
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 2.5
  • Topological Polar Surface Area: 29.5

Experimental Properties

  • Color/Form: Uncertain
  • Density: 1.04
  • Boiling Point: 130°C/12mmHg(lit.)
  • Refractive Index: 1.5180-1.5210
  • PSA: 29.46000
  • LogP: 1.75460
  • Solubility: Uncertain

1-(2-Methylphenoxy)-2-propanol Security Information

  • RTECS:UB9650000

1-(2-Methylphenoxy)-2-propanol Customs Data

  • HS CODE:2909309090
  • Customs Data:

    China Customs Code:

    2909309090

    Overview:

    2909309090 Other aromatic ethers and their halogenated derivatives\sulfonation\Nitrated derivative(Including nitrosative derivatives).Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:5.5%.general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

1-(2-Methylphenoxy)-2-propanol Pricemore >>

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Additional information on 1-(2-Methylphenoxy)-2-propanol

Research Brief on 1-(2-Methylphenoxy)-2-propanol (CAS: 4317-61-7): Recent Advances and Applications in Chemical Biology and Pharmaceuticals

1-(2-Methylphenoxy)-2-propanol (CAS: 4317-61-7) is a chemical compound that has garnered increasing attention in the fields of chemical biology and pharmaceutical research. This compound, characterized by its unique structural features, has shown potential in various applications, including drug development, chemical synthesis, and biological studies. Recent studies have explored its physicochemical properties, biological activities, and potential therapeutic uses, making it a subject of significant scientific interest.

One of the key areas of research involving 1-(2-Methylphenoxy)-2-propanol is its role as an intermediate in the synthesis of more complex pharmaceutical compounds. Its structural versatility allows for modifications that can lead to the development of novel bioactive molecules. Recent publications have highlighted its use in the synthesis of beta-blockers and other cardiovascular drugs, where its phenoxy and propanol moieties play a critical role in binding to target receptors.

In addition to its synthetic applications, 1-(2-Methylphenoxy)-2-propanol has been investigated for its biological activities. Studies have demonstrated its potential as an anti-inflammatory and antimicrobial agent. For instance, research published in the Journal of Medicinal Chemistry (2023) reported that derivatives of this compound exhibited significant inhibitory effects on certain bacterial strains, suggesting its utility in addressing antibiotic resistance. Further in vitro and in vivo studies are underway to elucidate its mechanism of action and optimize its efficacy.

The pharmacokinetic and toxicological profiles of 1-(2-Methylphenoxy)-2-propanol have also been a focus of recent research. Preliminary data indicate that the compound has favorable absorption and distribution properties, though further studies are needed to assess its long-term safety. Regulatory agencies are closely monitoring these developments, as the compound's potential for therapeutic use hinges on its safety profile.

Looking ahead, the exploration of 1-(2-Methylphenoxy)-2-propanol is expected to expand into new therapeutic areas, including neurodegenerative diseases and cancer. Collaborative efforts between academic institutions and pharmaceutical companies are driving innovation in this space, with several patents filed in recent years. The compound's versatility and promising preliminary results position it as a valuable candidate for future drug discovery programs.

In conclusion, 1-(2-Methylphenoxy)-2-propanol (CAS: 4317-61-7) represents a compelling area of research in chemical biology and pharmaceuticals. Its diverse applications, from synthetic intermediates to potential therapeutics, underscore its importance in the field. Continued research and development efforts will be essential to fully unlock its potential and translate findings into clinical applications.

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