Cas no 904325-91-3 (1,1'-Biphenyl, 3-chloro-4,4'-difluoro-)

1,1'-Biphenyl, 3-chloro-4,4'-difluoro- is a halogenated biphenyl derivative characterized by its unique substitution pattern, featuring chlorine and fluorine atoms at specific positions on the aromatic rings. This structural configuration enhances its utility as an intermediate in organic synthesis, particularly in the development of advanced materials and pharmaceuticals. The presence of both chloro and fluoro substituents imparts distinct electronic and steric properties, making it valuable for cross-coupling reactions and as a building block for liquid crystals or agrochemicals. Its high purity and stability under standard conditions ensure consistent performance in demanding applications. The compound is typically handled under controlled conditions due to its halogenated nature.
1,1'-Biphenyl, 3-chloro-4,4'-difluoro- structure
904325-91-3 structure
Product Name:1,1'-Biphenyl, 3-chloro-4,4'-difluoro-
CAS No:904325-91-3
MF:C12H7ClF2
MW:224.633789300919
CID:1954373
PubChem ID:138543718
Update Time:2025-10-31

1,1'-Biphenyl, 3-chloro-4,4'-difluoro- Chemical and Physical Properties

Names and Identifiers

    • 1,1'-Biphenyl, 3-chloro-4,4'-difluoro-
    • 2-chloro-1-fluoro-4-(4-fluorophenyl)benzene
    • SCHEMBL20898226
    • 3-Chloro-4,4'-difluoro-1,1'-biphenyl
    • 904325-91-3
    • EN300-691940
    • Inchi: 1S/C12H7ClF2/c13-11-7-9(3-6-12(11)15)8-1-4-10(14)5-2-8/h1-7H
    • InChI Key: UKYONYLOHKYCBH-UHFFFAOYSA-N
    • SMILES: ClC1=C(C=CC(=C1)C1C=CC(=CC=1)F)F

Computed Properties

  • Exact Mass: 224.0204342Da
  • Monoisotopic Mass: 224.0204342Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 1
  • Complexity: 202
  • 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: 4.4
  • Topological Polar Surface Area: 0?2

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Additional information on 1,1'-Biphenyl, 3-chloro-4,4'-difluoro-

Comprehensive Analysis of 1,1'-Biphenyl, 3-chloro-4,4'-difluoro- (CAS No. 904325-91-3): Properties, Applications, and Industry Trends

The compound 1,1'-Biphenyl, 3-chloro-4,4'-difluoro- (CAS No. 904325-91-3) is a halogen-substituted biphenyl derivative that has garnered significant attention in the fields of organic synthesis, materials science, and specialty chemicals. With its unique molecular structure featuring chloro and difluoro functional groups, this compound serves as a versatile intermediate for advanced applications. Researchers and industry professionals frequently search for terms like "biphenyl derivatives," "halogenated aromatic compounds," and "CAS 904325-91-3 applications," reflecting its growing relevance in innovation-driven sectors.

One of the most notable characteristics of 3-chloro-4,4'-difluorobiphenyl is its role in the development of high-performance materials. The compound's aromatic backbone and electron-withdrawing substituents make it an ideal candidate for designing liquid crystals, OLED (organic light-emitting diode) materials, and pharmaceutical intermediates. Recent trends in sustainable chemistry have also spurred interest in "green synthesis of halogenated biphenyls," with this compound being studied for atom-efficient catalytic reactions. Its thermal stability and compatibility with cross-coupling reactions (e.g., Suzuki-Miyaura) further enhance its utility in modern synthetic methodologies.

From an industrial perspective, 1,1'-Biphenyl, 3-chloro-4,4'-difluoro- aligns with the rising demand for "fine chemicals with low environmental impact." Analytical studies highlight its biodegradation pathways and potential for use in eco-friendly formulations—a topic frequently queried in academic and regulatory circles. The compound's spectral data (NMR, FT-IR) and crystallographic properties are well-documented, aiding in quality control for manufacturers. As industries prioritize "halogenated compound safety" and "REACH compliance," this biphenyl derivative stands out for its balanced performance-to-sustainability profile.

Emerging applications of CAS 904325-91-3 extend to the electronics sector, where its dielectric properties are explored for next-generation semiconductor coatings. Patent analyses reveal its incorporation into polymer matrices to enhance heat resistance—a critical factor for 5G and IoT devices. Meanwhile, the pharmaceutical industry investigates its scaffold for targeted drug delivery systems, leveraging the meta-chloro and para-fluoro substitutions for bioactive molecule design. These multidisciplinary uses address common search queries like "high-value biphenyl intermediates" and "specialty chemicals for advanced materials."

Quality standards for 3-chloro-4,4'-difluorobiphenyl are stringent, with HPLC purity thresholds exceeding 98% in commercial supplies. Suppliers emphasize batch-to-batch consistency through GC-MS validation, responding to market demands for "ultra-pure halogenated aromatics." Storage recommendations typically specify inert atmospheres to preserve the compound's stability, a detail often sought in "handling sensitive organic compounds" guidelines. As regulatory frameworks evolve, particularly concerning halogenated organic compounds, this substance's well-characterized toxicological profile positions it favorably for global supply chains.

Future research directions for 1,1'-Biphenyl, 3-chloro-4,4'-difluoro- may focus on catalytic fluorination techniques to improve synthesis efficiency—a hot topic in "organofluorine chemistry advancements." Computational modeling studies also predict its utility in designing metal-organic frameworks (MOFs), addressing searches for "functionalized linkers for porous materials." With the compound's patent landscape showing steady growth since 2015, its commercial trajectory reflects broader shifts toward tailored aromatic building blocks in high-tech industries.

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