Cas no 6311-66-6 (Phenol,4-(phenylmethoxy)-, 1-acetate)

Phenol,4-(phenylmethoxy)-, 1-acetate is a synthetic aromatic compound featuring a phenol core substituted with a benzyloxy group at the para position and an acetyl ester at the hydroxyl group. This structure imparts enhanced stability and controlled reactivity, making it useful in organic synthesis and specialty chemical applications. The acetyl group provides improved solubility in organic solvents, facilitating its use as an intermediate in pharmaceuticals, agrochemicals, and polymer chemistry. Its well-defined molecular architecture allows for selective functionalization, enabling precise modifications in multi-step synthetic routes. The compound’s stability under various conditions ensures consistent performance in industrial and research settings.
Phenol,4-(phenylmethoxy)-, 1-acetate structure
6311-66-6 structure
Product Name:Phenol,4-(phenylmethoxy)-, 1-acetate
CAS No:6311-66-6
MF:C15H14O3
MW:242.269864559174
CID:521036
Update Time:2026-04-29

Phenol,4-(phenylmethoxy)-, 1-acetate Chemical and Physical Properties

Names and Identifiers

    • Phenol,4-(phenylmethoxy)-, 1-acetate
    • 4-BENZYLOXYPHENYL ACETATE
    • 1-acetoxy-4-benzyloxy-benzene
    • 1-Acetoxy-4-benzyloxy-benzol
    • 4-(phenylMethoxy)
    • acetic acid 4-benzyloxy-phenyl ester
    • benzyl-(4-acetoxyphenyl)ether
    • p-Acetoxyphenylbenzylether
    • Inchi： InChI=1S/C15H14O3/c1-12(16)18-15-9-7-14(8-10-15)17-11-13-5-3-2-4-6-13/h2-10H,11H2,1H3
    • InChI Key： YNUDXDBNKZSVPT-UHFFFAOYSA-N
    • SMILES： CC(=O)OC1=CC=C(C=C1)OCC2=CC=CC=C2

Computed Properties

  • Exact Mass: 242.09400
  • Monoisotopic Mass: 242.094
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 5
  • Complexity: 251
  • 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: 3.5
  • Topological Polar Surface Area: 35.5A^2

Experimental Properties

  • Density: 1.144
  • Boiling Point: 369.6°C at 760 mmHg
  • Flash Point: 154.8°C
  • Refractive Index: 1.562
  • PSA: 35.53000
  • LogP: 3.19090

Phenol,4-(phenylmethoxy)-, 1-acetate Customs Data

  • HS CODE：2915390090
  • Customs Data：

    China Customs Code:

    2915390090

    Overview:

    2915390090. Other acetate esters. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods). MFN tariff:5.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Regulatory conditions:

    A.Customs clearance form for Inbound Goods
    B.Customs clearance form for outbound goods

    Inspection and quarantine category:

    R.Sanitary supervision and inspection of imported food
    S.Sanitary supervision and inspection of exported food
    M.Import commodity inspection
    N.Export commodity inspection

    Summary:

    2915390090. esters of acetic acid. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:5.5%. General tariff:30.0%

Phenol,4-(phenylmethoxy)-, 1-acetate Pricemore >>

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Phenol,4-(phenylmethoxy)-, 1-acetate Related Literature

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Additional information on Phenol,4-(phenylmethoxy)-, 1-acetate

Comprehensive Guide to Phenol,4-(phenylmethoxy)-, 1-acetate (CAS No. 6311-66-6): Properties, Applications, and Market Insights

Phenol,4-(phenylmethoxy)-, 1-acetate (CAS No. 6311-66-6) is a specialized organic compound widely used in the fragrance and pharmaceutical industries. This compound, also known as 4-Benzyloxyphenyl acetate, is valued for its unique chemical properties and versatility. In this article, we delve into its molecular structure, key applications, and emerging trends in the market, while addressing frequently searched questions about its uses and safety.

The molecular formula of Phenol,4-(phenylmethoxy)-, 1-acetate is C15H14O3, featuring a phenylmethoxy group attached to a phenol ring, which is further acetylated. This structure contributes to its stability and solubility in organic solvents, making it a preferred choice for synthetic applications. Researchers often explore its role as an intermediate in the synthesis of flavoring agents and aromatic compounds, aligning with the growing demand for sustainable and high-performance ingredients in cosmetics and perfumery.

One of the most searched questions about CAS No. 6311-66-6 is its application in fragrance formulations. Due to its mild, sweet aroma, this compound is frequently incorporated into perfumes, soaps, and lotions. Its ability to enhance scent longevity has made it a popular choice among manufacturers seeking to innovate in the clean beauty sector—a trending topic in consumer markets. Additionally, its compatibility with other esters and alcohols allows for tailored fragrance profiles, catering to niche preferences.

Beyond fragrances, Phenol,4-(phenylmethoxy)-, 1-acetate finds use in pharmaceutical research. Its acetyl group enables controlled release mechanisms, which are critical in drug delivery systems. Recent studies highlight its potential as a scaffold for anti-inflammatory and antioxidant derivatives, addressing the rising interest in natural therapeutics. This aligns with the surge in searches for "plant-based bioactive compounds" and "green chemistry solutions."

The market for CAS No. 6311-66-6 is expanding, driven by advancements in sustainable chemistry and regulatory shifts favoring eco-friendly ingredients. Analysts note increased procurement by European and North American manufacturers, particularly in the personal care and fine chemicals sectors. For buyers, understanding supply chain dynamics—such as pricing fluctuations due to raw material availability—is essential, as queried in search trends like "phenol derivatives market report 2024."

Safety and handling of 4-Benzyloxyphenyl acetate are also common search topics. While it is not classified as hazardous under standard regulations, proper storage in cool, dry environments is recommended to maintain stability. Material Safety Data Sheets (MSDS) emphasize its low reactivity, but users should adhere to general laboratory precautions, such as wearing gloves and goggles. These details cater to professionals seeking "safe handling of aromatic acetates" and "industrial chemical storage guidelines."

In summary, Phenol,4-(phenylmethoxy)-, 1-acetate (CAS No. 6311-66-6) is a multifaceted compound with significant industrial relevance. Its applications in fragrance science and pharmaceutical innovation reflect broader trends toward sustainability and health-conscious formulations. By addressing high-search-volume topics—from "green fragrance additives" to "phenol acetate derivatives"—this guide offers actionable insights for researchers, manufacturers, and marketers navigating the evolving chemical landscape.

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