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Atomfair 1-Iodo-4-propylbenzene C9H11I

Description 1-Iodo-4-propylbenzene (CAS No. 126261-84-5) is a high-purity aromatic organoiodine compound with the molecular formula C9H11I . This specialized chemical features a propyl group para-substituted with an iodine atom on a benzene ring, offering unique reactivity for cross-coupling reactions such as Suzuki, Negishi, and Stille couplings. With a molecular weight of 246.09 g/mol, it is a valuable intermediate in pharmaceutical synthesis, agrochemical development, and advanced material science. Our product is rigorously tested via GC, NMR, and HPLC to ensure ??98% purity, packaged under inert gas to prevent degradation. Ideal for researchers requiring precise stoichiometry in Pd-catalyzed transformations or radical-mediated functionalizations.

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Description

Description

1-Iodo-4-propylbenzene (CAS No. 126261-84-5) is a high-purity aromatic organoiodine compound with the molecular formula C9H11I. This specialized chemical features a propyl group para-substituted with an iodine atom on a benzene ring, offering unique reactivity for cross-coupling reactions such as Suzuki, Negishi, and Stille couplings. With a molecular weight of 246.09 g/mol, it is a valuable intermediate in pharmaceutical synthesis, agrochemical development, and advanced material science. Our product is rigorously tested via GC, NMR, and HPLC to ensure ??98% purity, packaged under inert gas to prevent degradation. Ideal for researchers requiring precise stoichiometry in Pd-catalyzed transformations or radical-mediated functionalizations.

  • CAS No: 126261-84-5
  • Molecular Formula: C9H11I
  • Molecular Weight: 246.09
  • Exact Mass: 245.99055
  • Monoisotopic Mass: 245.99055
  • IUPAC Name: 1-iodo-4-propylbenzene
  • SMILES: CCCC1=CC=C(C=C1)I
  • Synonyms: 1-Iodo-4-propylbenzene, 126261-84-5, 1-Iodo-4-n-propylbenzene, Benzene, 1-iodo-4-propyl-, 4-Iodopropylbenzene

Application

1-Iodo-4-propylbenzene serves as a key building block in transition-metal-catalyzed reactions for constructing complex biaryl architectures in drug discovery. It is utilized in liquid crystal synthesis due to its mesogenic properties and as a precursor for OLED materials. The compound also finds use in isotopic labeling studies and as a probe in mechanistic organic chemistry investigations.

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