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2-Phenyl-1-propanol (CAS 1123-85-9)

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CAS Number:
1123-85-9
Molecular Weight:
136.19
Molecular Formula:
CH3CH(C6H5)CH2OH
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Phenyl-1-propanol, a secondary alcohol with a phenyl group attached to the second carbon of the propanol chain, has been extensively studied in various research fields owing to its diverse applications and intriguing chemical properties. One significant area of interest lies in its utilization as a chiral building block in organic synthesis. Asymmetric synthesis methodologies often employ 2-phenyl-1-propanol as a chiral auxiliary or as a precursor for the synthesis of chiral ligands and catalysts due to the stereogenic center present in its structure. Researchers exploit the stereochemical properties of this compound to induce chirality and control the stereochemistry of target molecules during synthesis. Additionally, 2-phenyl-1-propanol has found applications in fragrance and flavor industries as a key component in the synthesis of aromatic compounds, owing to its characteristic aromatic profile derived from the phenyl moiety. Moreover, it serves as a starting material for the preparation of various pharmaceutical intermediates and fine chemicals. The versatile nature of 2-phenyl-1-propanol makes it a valuable tool in organic synthesis research, facilitating the development of novel compounds with potential applications in materials science, agrochemicals, and bioactive molecules.


2-Phenyl-1-propanol (CAS 1123-85-9) References

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  3. Poly(ethylene glycol)-lipase complexes that are highly active and enantioselective in ionic liquids.  |  Maruyama, T., et al. 2004. Org Biomol Chem. 2: 1239-44. PMID: 15064803
  4. Water dependent properties of cutinase in nonaqueous solvents: a computational study of enantioselectivity.  |  Micaelo, NM., et al. 2005. Biophys J. 89: 999-1008. PMID: 15923226
  5. Synergism between microwave irradiation and enzyme catalysis in transesterification of ethyl-3-phenylpropanoate with n-butanol.  |  Yadav, GD. and Pawar, SV. 2012. Bioresour Technol. 109: 1-6. PMID: 22305539
  6. Haloquadratum walsbyi Yields a Versatile, NAD+/NADP+ Dual Affinity, Thermostable, Alcohol Dehydrogenase (HwADH).  |  Cassidy, J. and Paradisi, F. 2018. Mol Biotechnol. 60: 420-426. PMID: 29654471
  7. [FAB (fast atom bombardment)-mass spectrometry. A new study method in the hands of the (forensic) toxicologist].  |  Gielsdorf, W. and Farrow, P. 1982. Z Rechtsmed. 89: 191-5. PMID: 7158081

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Phenyl-1-propanol, 5 g

sc-223456
5 g
$26.00