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Atomfair 2-(3,5-Dimethoxyphenyl)propan-2-ol C11H16O3

Description 2-(3,5-Dimethoxyphenyl)propan-2-ol (CAS No. 39507-96-5) is a high-purity organic compound with the molecular formula C11H16O3. This aromatic alcohol features a propan-2-ol group substituted at the 2-position of a 3,5-dimethoxyphenyl ring, offering unique reactivity and solubility properties. Ideal for pharmaceutical intermediates, organic synthesis, and material science research, this compound is characterized by its white to off-white crystalline appearance and excellent chemical stability. Packaged under inert conditions to ensure longevity, it is supplied with comprehensive analytical data including HPLC, GC-MS, and NMR for quality assurance. Store in a cool, dry place away from light and oxidizing agents.

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Description

Description

2-(3,5-Dimethoxyphenyl)propan-2-ol (CAS No. 39507-96-5) is a high-purity organic compound with the molecular formula C11H16O3. This aromatic alcohol features a propan-2-ol group substituted at the 2-position of a 3,5-dimethoxyphenyl ring, offering unique reactivity and solubility properties. Ideal for pharmaceutical intermediates, organic synthesis, and material science research, this compound is characterized by its white to off-white crystalline appearance and excellent chemical stability. Packaged under inert conditions to ensure longevity, it is supplied with comprehensive analytical data including HPLC, GC-MS, and NMR for quality assurance. Store in a cool, dry place away from light and oxidizing agents.

  • CAS No: 39507-96-5
  • Molecular Formula: C11H16O3
  • Molecular Weight: 196.24
  • Exact Mass: 196.109944368
  • Monoisotopic Mass: 196.109944368
  • IUPAC Name: 2-(3,5-dimethoxyphenyl)propan-2-ol
  • SMILES: CC(C)(C1=CC(=CC(=C1)OC)OC)O
  • Synonyms: 2-(3,5-Dimethoxyphenyl)propan-2-ol, 39507-96-5, Benzenemethanol, 3,5-dimethoxy-a,a-dimethyl-, 3,5-Dimethoxy-alpha,alpha-dimethylbenzyl alcohol, EINECS 254-476-1

Application

2-(3,5-Dimethoxyphenyl)propan-2-ol serves as a versatile building block in organic synthesis, particularly in the preparation of complex aromatic compounds. Researchers utilize it in the development of pharmaceuticals, agrochemicals, and specialty materials due to its reactive hydroxyl group and dimethoxy-substituted aromatic ring. Its stability and solubility make it suitable for coupling reactions and as a precursor in catalytic processes.

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