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Atomfair 6-iodo-3,4-dihydronaphthalen-1(2H)-one 6-iodo-1-tetralone C10H9IO

Description 6-Iodo-3,4-dihydronaphthalen-1(2H)-one (CAS No. 340825-13-0) is a high-purity organic compound with the molecular formula C10H9IO . This iodinated tetralone derivative is a valuable intermediate in synthetic organic chemistry, particularly in the construction of complex polycyclic frameworks. The compound features a reactive iodine substituent at the 6-position of the 3,4-dihydronaphthalen-1(2H)-one scaffold, making it a versatile building block for cross-coupling reactions and further functionalization. Available as a crystalline solid with >95% purity (HPLC), this product is rigorously tested to meet the stringent requirements of pharmaceutical and materials science research. Proper storage at 2-8??C under inert atmosphere is recommended to maintain stability.

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Description

Description

6-Iodo-3,4-dihydronaphthalen-1(2H)-one (CAS No. 340825-13-0) is a high-purity organic compound with the molecular formula C10H9IO. This iodinated tetralone derivative is a valuable intermediate in synthetic organic chemistry, particularly in the construction of complex polycyclic frameworks. The compound features a reactive iodine substituent at the 6-position of the 3,4-dihydronaphthalen-1(2H)-one scaffold, making it a versatile building block for cross-coupling reactions and further functionalization. Available as a crystalline solid with >95% purity (HPLC), this product is rigorously tested to meet the stringent requirements of pharmaceutical and materials science research. Proper storage at 2-8??C under inert atmosphere is recommended to maintain stability.

  • CAS No: 340825-13-0
  • Molecular Formula: C10H9IO
  • Molecular Weight: 272.08
  • Exact Mass: 271.96981
  • Monoisotopic Mass: 271.96981
  • IUPAC Name: 6-iodo-3,4-dihydro-2H-naphthalen-1-one
  • SMILES: C1CC2=C(C=CC(=C2)I)C(=O)C1
  • Synonyms: 6-iodo-3,4-dihydronaphthalen-1(2H)-one, 340825-13-0, 6-iodo-1-tetralone, 6-iodo-3,4-dihydro-2H-naphthalen-1-one, 6-iodo-1,2,3,4-tetrahydronaphthalen-1-one

Application

6-Iodo-3,4-dihydronaphthalen-1(2H)-one serves as a key precursor in the synthesis of biologically active tetralin derivatives through palladium-catalyzed coupling reactions. Researchers utilize this compound in medicinal chemistry programs targeting CNS disorders due to its privileged scaffold. The iodine moiety enables efficient derivatization via Buchwald-Hartwig amination or Suzuki-Miyaura cross-coupling for library generation. In materials science, it functions as a monomer for constructing conjugated polymers with optoelectronic properties.

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