Atomfair 2,4-Dichloro-7-iodoquinazoline C8H3Cl2IN2

Description 2,4-Dichloro-7-iodoquinazoline (CAS No. 796851-03-1) is a high-purity halogenated quinazoline derivative with the molecular formula C8H3Cl2IN2. This compound is a versatile building block in organic synthesis, particularly in the development of pharmaceutical intermediates and bioactive molecules. Its unique structure, featuring both chloro and iodo substituents on the quinazoline core, enables selective functionalization for targeted modifications. The product is supplied as a crystalline solid with ??95% purity (HPLC), ensuring optimal performance in cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed transformations. Ideal for researchers in medicinal chemistry and material science, it is packaged under inert conditions to guarantee stability and longevity.

Description

Description

2,4-Dichloro-7-iodoquinazoline (CAS No. 796851-03-1) is a high-purity halogenated quinazoline derivative with the molecular formula C8H3Cl2IN2. This compound is a versatile building block in organic synthesis, particularly in the development of pharmaceutical intermediates and bioactive molecules. Its unique structure, featuring both chloro and iodo substituents on the quinazoline core, enables selective functionalization for targeted modifications. The product is supplied as a crystalline solid with ??95% purity (HPLC), ensuring optimal performance in cross-coupling reactions, nucleophilic substitutions, and metal-catalyzed transformations. Ideal for researchers in medicinal chemistry and material science, it is packaged under inert conditions to guarantee stability and longevity.

  • CAS No: 796851-03-1
  • Molecular Formula: C8H3Cl2IN2
  • Molecular Weight: 324.93
  • Exact Mass: 323.87180
  • Monoisotopic Mass: 323.87180
  • IUPAC Name: 2,4-dichloro-7-iodoquinazoline
  • SMILES: C1=CC2=C(C=C1I)N=C(N=C2Cl)Cl
  • Synonyms: 2,4-DICHLORO-7-IODOQUINAZOLINE, 959237-34-4, 2,4-dichloro-7-iodo-quinazoline, MFCD09954872, SCHEMBL4178672

Application

2,4-Dichloro-7-iodoquinazoline serves as a key intermediate in the synthesis of kinase inhibitors and other heterocyclic compounds with potential therapeutic applications. Its reactive halogen sites facilitate Suzuki-Miyaura and Buchwald-Hartwig couplings for drug discovery pipelines. The compound is also employed in material science for constructing luminescent or electron-deficient aromatic systems. Researchers utilize it to explore structure-activity relationships in quinazoline-based scaffolds.

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