Cas no 55708-65-1 (4-Benzyl-oxy-3-methoxystyrene)

4-Benzyl-oxy-3-methoxystyrene is a styrene derivative featuring benzyloxy and methoxy functional groups at the 4- and 3-positions, respectively. This compound is commonly utilized as an intermediate in organic synthesis, particularly in the preparation of fine chemicals, pharmaceuticals, and specialty polymers. Its reactive vinyl group enables participation in polymerization reactions, while the electron-donating substituents enhance its utility in electrophilic aromatic substitution and cross-coupling reactions. The benzyloxy group also offers potential for further functionalization through deprotection. The compound is typically supplied as a high-purity solid, ensuring consistent performance in synthetic applications. Its structural features make it a versatile building block for advanced molecular architectures.
4-Benzyl-oxy-3-methoxystyrene structure
4-Benzyl-oxy-3-methoxystyrene structure
Product Name:4-Benzyl-oxy-3-methoxystyrene
CAS No:55708-65-1
MF:C16H16O2
MW:240.297044754028
CID:386285
PubChem ID:563567
Update Time:2025-05-26

4-Benzyl-oxy-3-methoxystyrene Chemical and Physical Properties

Names and Identifiers

    • Benzene,4-ethenyl-2-methoxy-1-(phenylmethoxy)-
    • 4-Benzyloxy-3-methoxystyrene
    • 4-ethenyl-2-methoxy-1-phenylmethoxybenzene
    • 1-benzyloxy-2-methoxy-4-vinylbenzene
    • 2-Benzyloxy-5-vinylanisole
    • 4-benzyloxy-3-methoxy-1-ethenylbenzene
    • 4-ethenyl-2-methoxy-1-benzyloxybenzene
    • DTXSID60204249
    • 55708-65-1
    • 4-Benzyloxy-3-methoxystyrene, 97%
    • FT-0617656
    • 4-Ethenyl-2-methoxy-1-(phenylmethoxy)benzene
    • EINECS 259-771-9
    • AKOS015889062
    • 1-(benzyloxy)-4-ethenyl-2-methoxybenzene
    • 1-(Benzyloxy)-2-methoxy-4-vinylbenzene
    • 7AJZ2PMJ94
    • Benzene, 4-ethenyl-2-methoxy-1-(phenylmethoxy)-
    • NS00033374
    • SCHEMBL348043
    • 1-(Benzyloxy)-2-methoxy-4-vinylbenzene #
    • 4-Benzyl-oxy-3-methoxystyrene
    • Inchi: 1S/C16H16O2/c1-3-13-9-10-15(16(11-13)17-2)18-12-14-7-5-4-6-8-14/h3-11H,1,12H2,2H3
    • InChI Key: DPAUCHAAEWIRKG-UHFFFAOYSA-N
    • SMILES: O(C1C=CC(C=C)=CC=1OC)CC1C=CC=CC=1

Computed Properties

  • Exact Mass: 240.11500
  • Monoisotopic Mass: 240.115
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 5
  • Complexity: 246
  • 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: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 18.5A^2

Experimental Properties

  • Color/Form: Not available
  • Density: 1.0752 (rough estimate)
  • Melting Point: 49-54?°C(lit.)
  • Boiling Point: 343.02°C (rough estimate)
  • Flash Point: >230?°F
  • Refractive Index: 1.6000 (estimate)
  • PSA: 18.46000
  • LogP: 3.91720
  • Solubility: Not available

4-Benzyl-oxy-3-methoxystyrene Security Information

  • WGK Germany:3
  • Safety Instruction: S24/25
  • Safety Term:S24/25

4-Benzyl-oxy-3-methoxystyrene Pricemore >>

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4-Benzyl-oxy-3-methoxystyrene Production Method

Additional information on 4-Benzyl-oxy-3-methoxystyrene

Professional Introduction to 4-Benzyl-oxy-3-methoxystyrene (CAS No. 55708-65-1)

4-Benzyl-oxy-3-methoxystyrene, with the chemical formula C14H13O2 and CAS number 55708-65-1, is a significant compound in the field of organic chemistry and pharmaceutical research. This compound belongs to the class of styrene derivatives, which are widely recognized for their diverse applications in polymer chemistry, material science, and medicinal chemistry. The presence of both a benzyl-oxy group and a methoxy substituent on the styrene backbone imparts unique chemical properties that make it a valuable intermediate in synthetic chemistry.

The structural features of 4-Benzyl-oxy-3-methoxystyrene contribute to its reactivity and utility in various chemical transformations. The benzyl-oxy group can participate in nucleophilic substitution reactions, while the methoxy group can serve as an electron-donating moiety, influencing the electronic properties of the aromatic ring. These characteristics make it a versatile building block for the synthesis of more complex molecules, including potential pharmacophores in drug development.

In recent years, there has been growing interest in the application of styrene derivatives in pharmaceutical research due to their ability to modulate biological pathways. For instance, studies have shown that certain stilbene derivatives exhibit antioxidant and anti-inflammatory properties, which are relevant to the treatment of chronic diseases such as cancer and neurodegenerative disorders. The compound 4-Benzyl-oxy-3-methoxystyrene has been explored as a precursor in the synthesis of these bioactive molecules, highlighting its importance in medicinal chemistry.

The synthesis of 4-Benzyl-oxy-3-methoxystyrene typically involves classical organic reactions such as etherification and substitution reactions. Advanced synthetic methodologies, including palladium-catalyzed cross-coupling reactions, have been employed to enhance yield and selectivity. These techniques are crucial for producing high-purity compounds suitable for further applications in drug discovery and material science.

One of the most compelling aspects of 4-Benzyl-oxy-3-methoxystyrene is its role as a key intermediate in the development of novel materials. Styrene derivatives are known for their ability to form polymers with desirable mechanical and thermal properties. Researchers have utilized 4-Benzyl-oxy-3-methoxystyrene to create advanced polymers that find applications in coatings, adhesives, and specialty plastics. The incorporation of functional groups like benzyl-oxy and methoxy allows for fine-tuning of material properties, making this compound indispensable in industrial applications.

The pharmaceutical industry has also leveraged the unique properties of 4-Benzyl-oxy-3-methoxystyrene in drug development. Its structural motif is reminiscent of natural products known for their biological activity, prompting investigations into its potential therapeutic effects. Preliminary studies have suggested that derivatives of this compound may exhibit antimicrobial and anticancer properties. These findings underscore the importance of exploring structurally diverse compounds like 4-Benzyl-oxy-3-methoxystyrene as lead candidates for new drugs.

In conclusion, 4-Benzyl-oxy-3-methoxystyrene (CAS No. 55708-65-1) is a multifaceted compound with significant implications in both synthetic chemistry and pharmaceutical research. Its unique structural features enable diverse applications ranging from polymer science to drug development. As research continues to uncover new uses for this compound, its importance is likely to grow further, solidifying its place as a cornerstone molecule in modern chemistry.

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