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CS-W001157 4
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(R)-4-Phenylbutan-2-ol

  • CAS No. 39516-03-5

  • Cat. No. CS-0179418
  • Purity≥98%
  • MDL No.MFCD03093081

*For research and further manufacturing use only, not for direct human use.

(R)-4-Phenylbutan-2-ol|CS-0179418

Structure of 39516-03-5

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General Information

  • CAS No. 39516-03-5
  • Cat. No. CS-0179418
  • Purity ≥98%
  • MDL No. MFCD03093081
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₄O
  • Molecular Weight 150.22
  • Synonym(s) (R)-4-Phenyl-2-butanol
  • SMILES O[C@H](C)CCC1=CC=CC=C1

Description

(R)-4-Phenylbutan-2-ol is a chiral alcohol featuring a benzylic stereocenter and a hydroxyl group at the C2 position. This bench-stable, moisture-tolerant compound integrates readily into asymmetric synthesis workflows. The phenyl substituent provides π-conjugation and steric bulk, enhancing selectivity in downstream transformations. Its defined stereochemistry supports precise molecular architecture in medicinal chemistry applications.

Application

(R)-4-Phenylbutan-2-ol serves as a valuable chiral building block in asymmetric synthesis, offering a well-defined stereocenter adjacent to a secondary alcohol. Its bench-stable nature and compatibility with standard functional group manipulations enable reliable use in the construction of pharmaceutical intermediates and bioactive heterocycles. The molecule functions effectively in oxidation, acylation, and coupling reactions, facilitating access to diverse stereochemically controlled scaffolds.

Safety Information

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GHS Pictogram :
GHS No : GHS05,GHS07
Signal Word : Danger
UN#: 1760
Class : 8
Packing Group : Ⅲ
Hazard Statements : H315-H318-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   20.23
  • LogP   2
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   3

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