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Atomfair 1-(4-Methoxyphenyl)propan-2-ol C10H14O2

Description 1-(4-Methoxyphenyl)propan-2-ol (CAS No. 30314-64-8) is a high-purity aromatic alcohol with the molecular formula C10H14O2. This compound features a methoxy-substituted phenyl ring attached to a propan-2-ol moiety, making it a versatile intermediate in organic synthesis and pharmaceutical research. It is supplied as a clear to pale-yellow liquid with a characteristic aromatic odor, ensuring optimal consistency for laboratory use. Suitable for chromatographic analysis, catalysis studies, and fine chemical applications, our product undergoes rigorous QC testing (including GC/MS and NMR) to guarantee ??98% purity. Packaged under inert gas in amber glass bottles to prevent degradation, it is ideal for researchers requiring reliable,…

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Description

Description

1-(4-Methoxyphenyl)propan-2-ol (CAS No. 30314-64-8) is a high-purity aromatic alcohol with the molecular formula C10H14O2. This compound features a methoxy-substituted phenyl ring attached to a propan-2-ol moiety, making it a versatile intermediate in organic synthesis and pharmaceutical research. It is supplied as a clear to pale-yellow liquid with a characteristic aromatic odor, ensuring optimal consistency for laboratory use. Suitable for chromatographic analysis, catalysis studies, and fine chemical applications, our product undergoes rigorous QC testing (including GC/MS and NMR) to guarantee ??98% purity. Packaged under inert gas in amber glass bottles to prevent degradation, it is ideal for researchers requiring reliable, high-quality building blocks for complex molecular architectures.

  • CAS No: 30314-64-8
  • Molecular Formula: C10H14O2
  • Molecular Weight: 166.22
  • Exact Mass: 166.099379685
  • Monoisotopic Mass: 166.099379685
  • IUPAC Name: 1-(4-methoxyphenyl)propan-2-ol
  • SMILES: CC(CC1=CC=C(C=C1)OC)O
  • Synonyms: 1-(4-methoxyphenyl)propan-2-ol, DTXSID20952673, DTXCID701380753, 817-110-7, 30314-64-8

Application

1-(4-Methoxyphenyl)propan-2-ol serves as a key synthetic intermediate in the preparation of pharmaceuticals, particularly in the development of adrenergic receptor agonists and fragrances. Its methoxy and hydroxyl functional groups enable participation in etherification, esterification, and condensation reactions. Researchers utilize this compound in asymmetric synthesis and chiral resolution studies due to its prochiral center.

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