Cas no 152434-86-1 (1-Benzyloxy-2,4-difluoro-benzene)

1-Benzyloxy-2,4-difluoro-benzene is a fluorinated aromatic compound featuring a benzyloxy substituent at the 1-position and fluorine atoms at the 2- and 4-positions. This structure imparts unique electronic and steric properties, making it a valuable intermediate in organic synthesis, particularly in pharmaceutical and agrochemical applications. The presence of fluorine enhances metabolic stability and lipophilicity, while the benzyloxy group offers reactivity for further functionalization. Its well-defined molecular architecture ensures consistent performance in cross-coupling reactions and as a building block for complex molecules. The compound is typically supplied in high purity, ensuring reliability in research and industrial processes.
1-Benzyloxy-2,4-difluoro-benzene structure
152434-86-1 structure
Product Name:1-Benzyloxy-2,4-difluoro-benzene
CAS No:152434-86-1
MF:C13H10F2O
MW:220.214710712433
MDL:MFCD12198257
CID:829540
PubChem ID:561269
Update Time:2025-06-14

1-Benzyloxy-2,4-difluoro-benzene Chemical and Physical Properties

Names and Identifiers

    • 1-(Benzyloxy)-2,4-difluorobenzene
    • Benzyl 2,4-difluorophenyl ether
    • 1-benzyloxy-2,4-dichloro-5-nitrobenzene
    • 1-benzyloxy-2,4-dichloro-5-nitro-benzene
    • 1-benzyloxy-2,4-difluoro-benzene
    • 4L-377S
    • ACMC-20ecic
    • Benzene, 1,5-dichloro-2-nitro-4-(phenylmethoxy)-
    • benzyldichloronitrophenylether
    • CTK0G1055
    • SureCN2568216
    • AN-584/43417514
    • 2,4-Difluorobenzene, 1-benzyloxy-
    • SCHEMBL412514
    • CGA43486
    • 2,4-difluoro-1-phenylmethoxybenzene
    • CS-0195346
    • E90712
    • AKOS017187542
    • 152434-86-1
    • DB-362949
    • 1-(Benzyloxy)-2,4-difluorobenzene #
    • MFCD12198257
    • 1-Benzyloxy-2,4-difluoro-benzene
    • MDL: MFCD12198257
    • Inchi: 1S/C13H10F2O/c14-11-6-7-13(12(15)8-11)16-9-10-4-2-1-3-5-10/h1-8H,9H2
    • InChI Key: SUJMBSRZMAZPOY-UHFFFAOYSA-N
    • SMILES: FC1C=C(C=CC=1OCC1C=CC=CC=1)F

Computed Properties

  • Exact Mass: 220.07
  • Monoisotopic Mass: 220.07
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 3
  • Complexity: 204
  • 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: 3.6
  • Topological Polar Surface Area: 9.2?2

1-Benzyloxy-2,4-difluoro-benzene Security Information

1-Benzyloxy-2,4-difluoro-benzene Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
B686928-10mg
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$ 50.00 2022-06-06
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$ 65.00 2022-06-06
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abcr
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abcr
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abcr
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Ambeed
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Additional information on 1-Benzyloxy-2,4-difluoro-benzene

Recent Advances in the Application of 1-Benzyloxy-2,4-difluoro-benzene (CAS: 152434-86-1) in Chemical and Biomedical Research

1-Benzyloxy-2,4-difluoro-benzene (CAS: 152434-86-1) is a fluorinated aromatic compound that has garnered significant attention in recent years due to its versatile applications in chemical synthesis and biomedical research. This compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty materials. Its unique structural features, including the presence of fluorine atoms and a benzyloxy group, make it a valuable building block for the development of novel bioactive molecules.

Recent studies have highlighted the role of 1-Benzyloxy-2,4-difluoro-benzene in the synthesis of fluorinated drug candidates. Fluorination is a common strategy in drug design to enhance metabolic stability, bioavailability, and binding affinity. Researchers have successfully utilized this compound to develop potential inhibitors of enzymes involved in inflammatory pathways, showcasing its utility in the design of next-generation anti-inflammatory agents.

In addition to its pharmaceutical applications, 1-Benzyloxy-2,4-difluoro-benzene has been employed in material science. Its incorporation into liquid crystal materials has been shown to improve thermal stability and optical properties, making it a promising candidate for advanced display technologies. Recent publications have demonstrated its efficacy in enhancing the performance of organic light-emitting diodes (OLEDs) and other optoelectronic devices.

From a synthetic chemistry perspective, the compound's reactivity has been extensively studied. Recent advancements in catalytic methods have enabled more efficient and selective transformations of 1-Benzyloxy-2,4-difluoro-benzene, reducing the need for harsh reaction conditions and improving yields. These developments are particularly relevant for large-scale industrial applications where cost-effectiveness and environmental considerations are paramount.

In the biomedical field, researchers have explored the potential of 1-Benzyloxy-2,4-difluoro-benzene derivatives as probes for biological imaging. The fluorine atoms in its structure make it suitable for 19F NMR studies, allowing for non-invasive tracking of molecular interactions in complex biological systems. This application has opened new avenues for understanding drug-target interactions and cellular processes at the molecular level.

Despite these promising developments, challenges remain in the widespread adoption of 1-Benzyloxy-2,4-difluoro-benzene-based technologies. Issues such as scalability of synthesis, potential toxicity of derivatives, and regulatory hurdles need to be addressed through continued research. Recent collaborative efforts between academia and industry aim to overcome these barriers and fully realize the compound's potential across multiple disciplines.

Looking forward, the unique properties of 1-Benzyloxy-2,4-difluoro-benzene position it as a compound of significant interest for future research. Its applications span from drug discovery to advanced materials, with ongoing studies exploring its use in emerging fields such as targeted drug delivery and smart materials. As synthetic methodologies continue to evolve and our understanding of structure-activity relationships deepens, this compound is likely to play an increasingly important role in chemical and biomedical innovation.

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