Description
4-Ethyl-4′-iodobiphenyl (CAS No. 17078-76-1) is a high-purity organic compound with the molecular formula C14H13I, widely used in advanced research and industrial applications. This biphenyl derivative features an ethyl group at the 4-position and an iodine substituent at the 4′-position, making it a valuable intermediate in organic synthesis, material science, and pharmaceutical development. Its well-defined structure and reactivity enable precise modifications for tailored applications.
Our product is rigorously tested to ensure ≥98% purity (HPLC/GC), with stringent quality control for consistency in research outcomes. Supplied in sealed, light-protected packaging to prevent degradation, it is ideal for use in cross-coupling reactions, liquid crystal formulations, and as a building block for complex molecular architectures. Suitable for academic, pharmaceutical, and industrial laboratories seeking reliable, high-performance reagents.
Properties
- CAS Number: 17078-76-1
- Complexity: 174
- IUPAC Name: 1-ethyl-4-(4-iodophenyl)benzene
- InChI: InChI=1S/C14H13I/c1-2-11-3-5-12(6-4-11)13-7-9-14(15)10-8-13/h3-10H,2H2,1H3
- InChI Key: DUQFCMVIJVWQMX-UHFFFAOYSA-N
- Exact Mass: 308.00620
- Molecular Formula: C14H13I
- Molecular Weight: 308.16
- SMILES: CCC1=CC=C(C=C1)C2=CC=C(C=C2)I
- Monoisotopic Mass: 308.00620
- Synonyms: 4-Ethyl-4′-iodobiphenyl, 17078-76-1, 1-ethyl-4-(4-iodophenyl)benzene, 4-Ethyl-4′-iodo-1,1′-biphenyl, 4-Ethyl-4′-iodo-biphenyl, 4-ETHYL-4/’-IODOBIPHENYL, 4-Iodo-4′-ethylbiphenyl, MFCD03427551, SCHEMBL455526, SCHEMBL7102517, SCHEMBL15063621, DTXSID00573143, AKOS015911444, BS-52285, CS-0448237, E78428
Application
4-Ethyl-4′-iodobiphenyl serves as a key intermediate in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions, enabling the synthesis of extended π-conjugated systems for optoelectronic materials. It is also employed in the development of liquid crystals for display technologies due to its rigid biphenyl core and substituent effects. Researchers utilize this compound in medicinal chemistry to construct iodine-labeled analogs for imaging and pharmacokinetic studies.
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