Atomfair 3,5-Dichlorobenzylic alcohol C7H6Cl2O

Description 3,5-Dichlorobenzylic Alcohol (CAS No. 60211-57-6) is a high-purity chlorinated aromatic alcohol with the molecular formula C7H6Cl2O and IUPAC name (3,5-dichlorophenyl)methanol . This compound is a versatile intermediate in organic synthesis, characterized by its white to off-white crystalline appearance and stability under standard laboratory conditions. It is soluble in common organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), making it suitable for a wide range of chemical reactions. Ideal for researchers in pharmaceuticals, agrochemicals, and material science, this product is rigorously tested for purity (typically ??95-98% by GC/HPLC) and is available in customizable quantities. Proper storage in a…

Description

Description

3,5-Dichlorobenzylic Alcohol (CAS No. 60211-57-6) is a high-purity chlorinated aromatic alcohol with the molecular formula C7H6Cl2O and IUPAC name (3,5-dichlorophenyl)methanol. This compound is a versatile intermediate in organic synthesis, characterized by its white to off-white crystalline appearance and stability under standard laboratory conditions. It is soluble in common organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), making it suitable for a wide range of chemical reactions. Ideal for researchers in pharmaceuticals, agrochemicals, and material science, this product is rigorously tested for purity (typically ??95-98% by GC/HPLC) and is available in customizable quantities. Proper storage in a cool, dry place is recommended to maintain its integrity.

  • CAS No: 60211-57-6
  • Molecular Formula: C7H6Cl2O
  • Molecular Weight: 177.02
  • Exact Mass: 175.9795702
  • Monoisotopic Mass: 175.9795702
  • IUPAC Name: (3,5-dichlorophenyl)methanol
  • SMILES: C1=C(C=C(C=C1Cl)Cl)CO
  • Synonyms: 3,5-DICHLOROBENZYL ALCOHOL, 60211-57-6, 3,5-Dichlorobenzylic alcohol, EINECS 262-109-1, DTXSID10208959

Application

3,5-Dichlorobenzylic Alcohol is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a precursor for the production of fungicides, herbicides, and biologically active compounds due to its reactive benzylic hydroxyl group. Researchers also utilize it in the development of polymer additives and corrosion inhibitors. Its chlorinated aromatic structure makes it valuable in cross-coupling reactions and as a building block for more complex molecules.

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