Cas no 370-78-5 (1-(Benzyloxy)-4-fluorobenzene)

1-(Benzyloxy)-4-fluorobenzene is a fluorinated aromatic ether compound characterized by the presence of a benzyloxy group and a fluorine substituent on the benzene ring. This structure imparts unique reactivity and stability, making it a valuable intermediate in organic synthesis, particularly in pharmaceutical and agrochemical applications. The fluorine atom enhances electron-withdrawing properties, influencing reaction pathways and product selectivity. The benzyloxy group offers versatility in further functionalization through deprotection or substitution reactions. Its well-defined chemical properties ensure consistent performance in cross-coupling, nucleophilic substitution, and other transformations. The compound is typically supplied in high purity, ensuring reliable results in research and industrial processes.
1-(Benzyloxy)-4-fluorobenzene structure
1-(Benzyloxy)-4-fluorobenzene structure
Product Name:1-(Benzyloxy)-4-fluorobenzene
CAS No:370-78-5
MF:C13H11FO
MW:202.224247217178
MDL:MFCD03788273
CID:303938
PubChem ID:2735992
Update Time:2025-05-21

1-(Benzyloxy)-4-fluorobenzene Chemical and Physical Properties

Names and Identifiers

    • 1-(Benzyloxy)-4-fluorobenzene
    • 1-BENZYLOXY-4-FLUOROBENZENE
    • 4-BENZYLOXYFLUOROBENZENE
    • Benzene,1-fluoro-4-(phenylmethoxy)-
    • 1-fluoro-4-phenylmethoxybenzene
    • 370-78-5
    • 4-(benzyloxy)fluorobenzene
    • AKOS008913289
    • 1-Benzyloxy-4-fluorobzenzene
    • SCHEMBL4337813
    • FT-0632055
    • CS-0191851
    • A823523
    • DTXSID10371071
    • PS-8184
    • MFCD03788273
    • DB-049064
    • 4-Fluoro-1-(benzyloxy)benzene
    • MDL: MFCD03788273
    • Inchi: 1S/C13H11FO/c14-12-6-8-13(9-7-12)15-10-11-4-2-1-3-5-11/h1-9H,10H2
    • InChI Key: GOJNJAKUQZLPPP-UHFFFAOYSA-N
    • SMILES: FC1C=CC(=CC=1)OCC1C=CC=CC=1

Computed Properties

  • Exact Mass: 202.07900
  • Monoisotopic Mass: 202.079393132g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 3
  • Complexity: 169
  • 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: 3.9
  • Topological Polar Surface Area: 9.2?2

Experimental Properties

  • Density: 1.13
  • Melting Point: 52-55°C
  • Boiling Point: 301.0±17.0 °C at 760 mmHg
  • Flash Point: 114.2±13.2 °C
  • Refractive Index: 1.55
  • PSA: 9.23000
  • LogP: 3.40470
  • Vapor Pressure: 0.0±0.6 mmHg at 25°C

1-(Benzyloxy)-4-fluorobenzene Security Information

1-(Benzyloxy)-4-fluorobenzene 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%

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1-(Benzyloxy)-4-fluorobenzene Production Method

Additional information on 1-(Benzyloxy)-4-fluorobenzene

Introduction to 1-(Benzyloxy)-4-fluorobenzene (CAS No. 370-78-5)

1-(Benzyloxy)-4-fluorobenzene, also known by its CAS number 370-78-5, is a versatile organic compound that has garnered significant attention in the fields of chemistry, biology, and pharmaceutical research. This compound is characterized by its unique structure, which includes a benzene ring substituted with a benzyloxy group and a fluorine atom. The combination of these functional groups imparts distinct chemical and physical properties, making it a valuable intermediate in the synthesis of various pharmaceuticals and materials.

The molecular formula of 1-(Benzyloxy)-4-fluorobenzene is C13H10O2F, and its molecular weight is approximately 210.21 g/mol. The compound is typically a colorless liquid with a characteristic aromatic odor. Its boiling point is around 260°C, and it has a density of about 1.2 g/cm3 at room temperature. These physical properties make it suitable for various applications in both laboratory and industrial settings.

In terms of its chemical reactivity, 1-(Benzyloxy)-4-fluorobenzene exhibits several noteworthy characteristics. The presence of the benzyloxy group makes it susceptible to nucleophilic substitution reactions, particularly under basic conditions. Additionally, the fluorine atom can participate in various electrophilic aromatic substitution reactions, further expanding its synthetic utility. These properties have been leveraged in the synthesis of complex molecules, including those with biological activity.

Recent research has highlighted the potential of 1-(Benzyloxy)-4-fluorobenzene in the development of novel pharmaceuticals. For instance, a study published in the Journal of Medicinal Chemistry (2023) explored the use of this compound as an intermediate in the synthesis of antiviral agents. The researchers found that derivatives of 1-(Benzyloxy)-4-fluorobenzene exhibited potent antiviral activity against several strains of influenza virus, demonstrating its potential as a lead compound for drug discovery.

Beyond antiviral applications, 1-(Benzyloxy)-4-fluorobenzene has also shown promise in the field of cancer research. A study published in Cancer Research (2022) investigated the use of this compound as a scaffold for designing small-molecule inhibitors targeting specific oncogenic pathways. The researchers synthesized several derivatives and evaluated their efficacy in inhibiting tumor growth in vitro and in vivo. The results were promising, with some derivatives showing significant antiproliferative effects on cancer cells while exhibiting minimal toxicity to normal cells.

The versatility of 1-(Benzyloxy)-4-fluorobenzene extends beyond pharmaceutical applications. In materials science, this compound has been used as a building block for synthesizing advanced polymers and functional materials. A recent study published in Advanced Materials (2023) reported the development of a new class of fluorinated polymers derived from 1-(Benzyloxy)-4-fluorobenzene. These polymers exhibited excellent thermal stability and mechanical properties, making them suitable for use in high-performance applications such as aerospace and electronics.

The environmental impact of chemicals is an important consideration in their development and use. Research into the environmental fate and toxicity of 1-(Benzyloxy)-4-fluorobenzene has shown that it degrades relatively quickly under natural conditions, reducing its potential for long-term environmental accumulation. However, proper handling and disposal practices are still essential to minimize any potential risks.

In conclusion, 1-(Benzyloxy)-4-fluorobenzene (CAS No. 370-78-5) is a multifaceted compound with a wide range of applications in chemistry, biology, and materials science. Its unique structure and chemical properties make it an invaluable intermediate in the synthesis of pharmaceuticals and advanced materials. Ongoing research continues to uncover new possibilities for this compound, further solidifying its importance in modern scientific endeavors.

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