Description

3,5-Difluoro-1,4-pentyl-1,1,2,3,4,5,6-hexahydro-1,1,2:2,4,3-terphenyl (CAS No. 137528-84-8) is a high-purity fluorinated terphenyl derivative with the molecular formula C₂₃H₂₈F₂. This compound features a unique structural arrangement comprising a pentyl-substituted cyclohexylphenyl core and a difluorobenzene moiety, making it an excellent candidate for advanced material science and liquid crystal applications. Its precise synthesis and rigorous quality control ensure optimal performance in research and industrial settings. Suitable for use in organic synthesis, photochemistry, and optoelectronic material development, this compound is available in various quantities to meet both laboratory-scale and bulk requirements. Packaged under inert conditions to guarantee stability and longevity.

Properties

• CAS Number: 137528-84-8
• Complexity: 356
• IUPAC Name: 1,3-difluoro-5-[4-(4-pentylcyclohexyl)phenyl]benzene
• InChI: InChI=1S/C23H28F2/c1-2-3-4-5-17-6-8-18(9-7-17)19-10-12-20(13-11-19)21-14-22(24)16-23(25)15-21/h10-18H,2-9H2,1H3
• InChI Key: WVHQVIBUBHGQDE-UHFFFAOYSA-N
• Exact Mass: 342.21590722
• Molecular Formula: C23H28F2
• Molecular Weight: 342.5
• SMILES: CCCCCC1CCC(CC1)C2=CC=C(C=C2)C3=CC(=CC(=C3)F)F
• Monoisotopic Mass: 342.21590722
• Synonyms: 137528-84-8, DTXSID10718083, 3~3~,3~5~-Difluoro-1~4~-pentyl-1~1~,1~2~,1~3~,1~4~,1~5~,1~6~-hexahydro-1~1~,2~1~:2~4~,3~1~-terphenyl, DTXCID80668829, SCHEMBL9224215, SCHEMBL9224220

Application

This compound is primarily utilized in the development of liquid crystal materials due to its stable mesomorphic properties and fluorinated aromatic structure. It serves as a key intermediate in the synthesis of advanced organic electronic materials, including OLEDs and photovoltaic devices. Researchers also employ it in studies of fluorinated aromatic systems for their unique electronic and steric effects.

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