Cas no 501-92-8 (4-Allylphenol)

4-Allylphenol is a phenolic compound characterized by the presence of an allyl group (–CH?CH=CH?) attached to a phenol ring. This structure imparts reactivity suitable for applications in polymer chemistry, organic synthesis, and specialty chemical formulations. Its allyl group enables participation in reactions such as radical polymerization, thiol-ene coupling, and electrophilic substitutions, making it a versatile intermediate. The phenolic hydroxyl group further enhances its utility in crosslinking reactions or as a precursor for derivatives like allyl ethers. 4-Allylphenol exhibits moderate solubility in organic solvents and stability under standard conditions, facilitating handling in industrial and laboratory settings. Its dual functionality supports its use in adhesives, coatings, and resin systems.
4-Allylphenol structure
4-Allylphenol structure
Product Name:4-Allylphenol
CAS No:501-92-8
MF:C9H10O
MW:134.175102710724
MDL:MFCD01940501
CID:368060
Update Time:2025-06-11

4-Allylphenol Chemical and Physical Properties

Names and Identifiers

    • Phenol,4-(2-propen-1-yl)-
    • 4-Allylphenol
    • 4-prop-2-enylphenol
    • 1-allyl-4-hydroxybenzene
    • 4-(2-propenyl)phenol
    • 4-(prop-2-enyl)phenol
    • Chavicol
    • p-Allylphenol
    • Phenol,4-(2-propenyl)
    • Phenol,p-allyl
    • p-Hydroxyallylbenzene
    • Phenol, 4-(2-propenyl)-
    • p-Chavicol
    • 4-(prop-2-en-1-yl)phenol
    • Phenol, p-allyl-
    • gamma-(p-Hydroxyphenyl)-alpha-propylene
    • 4-(Prop-2-enyl)-phenol
    • 3-(4-Hydroxyphenyl)-1-propene
    • Phenol, p-allyl- (8CI)
    • .gamma.-(p-Hydroxyphenyl)-.alpha.-propylene
    • RGIBXDHONMXTLI-UHFFFAOYSA-N
    • Q5ER4K6969
    • Phenol, 4-(2-propenyl)- (9CI)
    • alpha -propylene
    • p
    • MDL: MFCD01940501
    • Inchi: 1S/C9H10O/c1-2-3-8-4-6-9(10)7-5-8/h2,4-7,10H,1,3H2
    • InChI Key: RGIBXDHONMXTLI-UHFFFAOYSA-N
    • SMILES: OC1C=CC(CC=C)=CC=1

Computed Properties

  • Exact Mass: 134.07300
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 101
  • 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
  • Surface Charge: 0
  • Tautomer Count: 2
  • XLogP3: 2.9
  • Topological Polar Surface Area: 20.2

Experimental Properties

  • Color/Form: liquid
  • Density: d415 1.0203; d420 1.0175
  • Melting Point: 15.8°
  • Boiling Point: bp760 238°; bp16 123°
  • Refractive Index: nD18 1.5441
  • PSA: 20.23000
  • LogP: 2.12070
  • FEMA: 4075 | 4-ALLYLPHENOL
  • Solubility: Soluble in ethanol, ether, chloroform, petroleum ether, etc.

4-Allylphenol Security Information

4-Allylphenol Customs Data

  • HS CODE:2907199090
  • Customs Data:

    China Customs Code:

    2907199090

    Overview:

    2907199090 Other monophenols. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2907199090 other monophenols VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

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4-Allylphenol Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:501-92-8)4-Allylphenol
Order Number:A917800
Stock Status:in Stock
Quantity:5g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 13:04
Price ($):437.0

Additional information on 4-Allylphenol

Recent Advances in the Study of 4-Allylphenol (CAS: 501-92-8) in Chemical Biology and Pharmaceutical Research

4-Allylphenol (CAS: 501-92-8) is a phenolic compound that has garnered significant attention in recent years due to its diverse biological activities and potential applications in pharmaceutical and chemical biology research. This compound, characterized by an allyl group attached to a phenol ring, exhibits unique chemical properties that make it a valuable scaffold for drug development and biochemical studies. Recent studies have explored its roles as an antioxidant, antimicrobial agent, and potential therapeutic candidate for various diseases.

One of the most notable advancements in the study of 4-Allylphenol is its demonstrated antioxidant properties. A 2023 study published in the Journal of Medicinal Chemistry highlighted its ability to scavenge reactive oxygen species (ROS) and protect cells from oxidative stress. The research team employed in vitro assays and molecular docking simulations to elucidate the mechanism behind its antioxidant activity, revealing that 4-Allylphenol interacts with key enzymes involved in oxidative pathways, such as NADPH oxidase and superoxide dismutase.

In addition to its antioxidant effects, 4-Allylphenol has shown promising antimicrobial activity. A recent investigation published in Bioorganic & Medicinal Chemistry Letters reported its efficacy against a range of Gram-positive and Gram-negative bacteria, including Staphylococcus aureus and Escherichia coli. The study attributed this activity to the compound's ability to disrupt bacterial cell membranes and inhibit essential metabolic pathways. These findings suggest that 4-Allylphenol could serve as a lead compound for the development of novel antibiotics.

Another area of interest is the potential therapeutic applications of 4-Allylphenol in cancer research. A 2022 study in Cancer Research demonstrated that 4-Allylphenol induces apoptosis in certain cancer cell lines by modulating the expression of pro-apoptotic proteins such as Bax and caspase-3. The researchers also observed synergistic effects when 4-Allylphenol was combined with conventional chemotherapeutic agents, indicating its potential as an adjunct therapy in oncology.

Despite these promising findings, challenges remain in the clinical translation of 4-Allylphenol. Issues such as bioavailability, metabolic stability, and potential toxicity need to be addressed through further preclinical and clinical studies. Recent efforts have focused on structural modifications of 4-Allylphenol to enhance its pharmacokinetic properties while retaining its biological activity. For instance, a 2023 study in European Journal of Medicinal Chemistry reported the synthesis of 4-Allylphenol derivatives with improved solubility and reduced cytotoxicity.

In conclusion, 4-Allylphenol (CAS: 501-92-8) represents a versatile compound with significant potential in chemical biology and pharmaceutical research. Its multifaceted biological activities, ranging from antioxidant and antimicrobial effects to anticancer properties, make it a compelling subject for further investigation. Future research should focus on optimizing its chemical structure, elucidating its mechanisms of action, and evaluating its safety and efficacy in clinical settings. As the field progresses, 4-Allylphenol may emerge as a key player in the development of novel therapeutic agents.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:501-92-8)4-Allylphenol
A917800
Purity:99%
Quantity:5g
Price ($):437.0
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