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Atomfair 2,3-Dichloroanisole C7H6Cl2O

Description 2,3-Dichloroanisole (CAS No. 1984-59-4) is a high-purity chlorinated aromatic compound with the molecular formula C7H6Cl2O and IUPAC name 1,2-dichloro-3-methoxybenzene . This specialty chemical is widely utilized in organic synthesis, agrochemical research, and pharmaceutical development due to its reactive dichloro and methoxy functional groups. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed, light-resistant containers to maintain stability. Ideal as a building block for heterocyclic compounds, 2,3-Dichloroanisole exhibits excellent solubility in common organic solvents like ethanol, acetone, and dichloromethane. Available in research quantities from 100mg to 10kg batches, with optional custom purity and packaging…

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Description

Description

2,3-Dichloroanisole (CAS No. 1984-59-4) is a high-purity chlorinated aromatic compound with the molecular formula C7H6Cl2O and IUPAC name 1,2-dichloro-3-methoxybenzene. This specialty chemical is widely utilized in organic synthesis, agrochemical research, and pharmaceutical development due to its reactive dichloro and methoxy functional groups. Our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed, light-resistant containers to maintain stability. Ideal as a building block for heterocyclic compounds, 2,3-Dichloroanisole exhibits excellent solubility in common organic solvents like ethanol, acetone, and dichloromethane. Available in research quantities from 100mg to 10kg batches, with optional custom purity and packaging configurations.

  • CAS No: 1984-59-4
  • Molecular Formula: C7H6Cl2O
  • Molecular Weight: 177.02
  • Exact Mass: 175.9795702
  • Monoisotopic Mass: 175.9795702
  • IUPAC Name: 1,2-dichloro-3-methoxybenzene
  • SMILES: COC1=C(C(=CC=C1)Cl)Cl
  • Synonyms: 2,3-Dichloroanisole, 1984-59-4, 1,2-Dichloro-3-methoxybenzene, Benzene, 1,2-dichloro-3-methoxy-, EINECS 217-853-1

Application

2,3-Dichloroanisole serves as a key intermediate in the synthesis of advanced agrochemicals, particularly for crop protection agents. Researchers employ this compound in palladium-catalyzed cross-coupling reactions to construct complex aromatic systems. In pharmaceutical development, it functions as a precursor for antimicrobial and antifungal agents. The compound’s electron-withdrawing chlorine atoms make it valuable for studying structure-activity relationships in medicinal chemistry.

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