Description

3-Fluoro-4′-propylbiphenyl (CAS No. 948044-01-7) is a high-purity organic compound with the molecular formula C₁₅H₁₅F. This fluorinated biphenyl derivative is characterized by its unique structure, featuring a fluorine substituent at the 3-position and a propyl group at the 4′-position of the biphenyl scaffold. It is an invaluable intermediate for synthetic organic chemistry, particularly in the development of liquid crystals, pharmaceuticals, and advanced materials. With a molecular weight of 214.28 g/mol, this compound exhibits excellent stability and compatibility for use in research and industrial applications. Available in various quantities, our product is rigorously tested to ensure ≥95% purity (HPLC/GC), making it ideal for precision-driven scientific work.

Properties

• CAS Number: 948044-01-7
• Complexity: 194
• IUPAC Name: 1-fluoro-3-(4-propylphenyl)benzene
• InChI: InChI=1S/C15H15F/c1-2-4-12-7-9-13(10-8-12)14-5-3-6-15(16)11-14/h3,5-11H,2,4H2,1H3
• InChI Key: HBTYBYGYVNHHBF-UHFFFAOYSA-N
• Exact Mass: 214.115778641
• Molecular Formula: C15H15F
• Molecular Weight: 214.28
• SMILES: CCCC1=CC=C(C=C1)C2=CC(=CC=C2)F
• Monoisotopic Mass: 214.115778641
• Synonyms: 948044-01-7, 3-fluoro-4′-propylbiphenyl, 4′-PROPYL-3-FLUORO-1,1′-BIPHENYL, 1-fluoro-3-(4-propylphenyl)benzene, SCHEMBL502700, SCHEMBL8088884, SCHEMBL10435172, SCHEMBL15063626, SCHEMBL27900192, HBTYBYGYVNHHBF-UHFFFAOYSA-N, DTXSID501301052, 1-(3-fluorophenyl)-4-propylbenzene, 3-fluoro-1-(4-propylphenyl)benzene, AKOS040767702, 3-Fluoro-4a(2)-propyl-1,1a(2)-biphenyl, EN300-842893

Application

3-Fluoro-4′-propylbiphenyl is widely utilized as a key building block in the synthesis of liquid crystal materials for display technologies. Its fluorinated biphenyl core contributes to the modulation of mesophase behavior and thermal stability in liquid crystal mixtures. Researchers also employ this compound in organic electronics and as a precursor for pharmaceutical intermediates. Additionally, it serves as a model substrate in studies of cross-coupling reactions and aromatic fluorination methodologies.

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