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Atomfair 4,4′-Diiodobiphenyl C12H8I2

Description 4,4′-Diiodobiphenyl (CAS No. 3001-15-8) is a high-purity aromatic compound with the molecular formula C12H8I2and IUPAC name 1-iodo-4-(4-iodophenyl)benzene . This crystalline solid is widely utilized in organic synthesis, material science, and pharmaceutical research due to its versatile reactivity as a halogenated biphenyl derivative. Our product is rigorously tested to ensure exceptional quality, with purity levels suitable for advanced research applications. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex biaryl structures. The compound’s high iodine content also makes it valuable for X-ray contrast agents and liquid crystal displays (LCDs). Proper handling under inert conditions…

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Description

Description

4,4′-Diiodobiphenyl (CAS No. 3001-15-8) is a high-purity aromatic compound with the molecular formula C12H8I2 and IUPAC name 1-iodo-4-(4-iodophenyl)benzene. This crystalline solid is widely utilized in organic synthesis, material science, and pharmaceutical research due to its versatile reactivity as a halogenated biphenyl derivative. Our product is rigorously tested to ensure exceptional quality, with purity levels suitable for advanced research applications. It serves as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex biaryl structures. The compound’s high iodine content also makes it valuable for X-ray contrast agents and liquid crystal displays (LCDs). Proper handling under inert conditions is recommended due to its sensitivity to light and moisture.

  • CAS No: 3001-15-8
  • Molecular Formula: C12H8I2
  • Molecular Weight: 406.00
  • Exact Mass: 405.87155
  • Monoisotopic Mass: 405.87155
  • IUPAC Name: 1-iodo-4-(4-iodophenyl)benzene
  • SMILES: C1=CC(=CC=C1C2=CC=C(C=C2)I)I
  • Synonyms: 4,4′-Diiodobiphenyl, 4,4′-Diiodo-1,1′-biphenyl, 1,1′-Biphenyl, 4,4′-diiodo-, 4,4′-Diiododiphenyl, EINECS 221-080-5

Application

4,4′-Diiodobiphenyl is extensively used as a building block in palladium-catalyzed cross-coupling reactions for synthesizing conjugated polymers and organic electronic materials. It finds applications in the development of liquid crystals for display technologies due to its rigid biphenyl core and halogen substituents. Researchers also employ this compound in medicinal chemistry for creating iodine-containing drug candidates and radiopharmaceuticals.

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