Description
4-Cyano-3,5-difluorophenyl 4-(but-3-en-1-yl)benzoate (CAS No. 208528-35-2) is a high-purity specialty chemical with the molecular formula C18H13F2NO2. This compound features a unique molecular structure combining a cyano-substituted difluorophenyl group and a butenyl-substituted benzoate ester, making it a valuable intermediate in advanced organic synthesis and material science applications. Its precise IUPAC name is (4-cyano-3,5-difluorophenyl) 4-but-3-enylbenzoate. Ideal for researchers and industrial chemists, this product is rigorously tested for purity and consistency, ensuring reliable performance in sensitive reactions. Available in customizable quantities with detailed technical documentation including NMR, HPLC, and MSDS data.
Properties
- CAS Number: 208528-35-2
- Complexity: 453
- IUPAC Name: (4-cyano-3,5-difluoro-phenyl) 4-but-3-enylbenzoate
- InChI: InChI=1S/C18H13F2NO2/c1-2-3-4-12-5-7-13(8-6-12)18(22)23-14-9-16(19)15(11-21)17(20)10-14/h2,5-10H,1,3-4H2
- InChI Key: KHEMMXMPDOTLHG-UHFFFAOYSA-N
- Exact Mass: 313.09143498
- Molecular Formula: C18H13F2NO2
- Molecular Weight: 313.3
- SMILES: C=CCCC1=CC=C(C=C1)C(=O)OC2=CC(=C(C(=C2)F)C#N)F
- Topological: 50.1
- Monoisotopic Mass: 313.09143498
- Synonyms: 208528-35-2, 4-Cyano-3,5-difluorophenyl 4-(but-3-en-1-yl)benzoate, Benzoic acid, 4-(3-buten-1-yl)-, 4-cyano-3,5-difluorophenyl ester, 4-cyano-3,5-difluorophenyl 4-(but-3-enyl)benzoate, BeBzodFCP, (4-cyano-3,5-difluorophenyl) 4-but-3-enylbenzoate, 4-Cyano-3,5-difluorophenyl 4-but-3-en-1-ylbenzoate, SCHEMBL13198968, C18H13F2NO2, DTXSID80609156, KHEMMXMPDOTLHG-UHFFFAOYSA-N, 4-(3-Butenyl)benzoic acid 4-cyano-3,5-difluorophenyl ester, MFCD34533609, BS-48254, DB-206009, E85297
Application
This compound serves as a versatile building block in the synthesis of liquid crystals and advanced polymeric materials, particularly for optoelectronic applications. Its fluorinated aromatic core and reactive ester group enable precise modifications in pharmaceutical intermediates and agrochemical derivatives. Researchers also utilize it in cross-coupling reactions to develop novel organic semiconductors. The butenyl side chain offers additional functionalization potential for polymer grafting or click chemistry.
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