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(R)-(+)-1-Phenylethanol, 99%, ee 97+%
(R)-(+)-1-Phenylethanol, 99%, ee 97+%
(R)-(+)-1-Phenylethanol, 99%, ee 97+%
Thermo Scientific Chemicals

(R)-(+)-1-Phenylethanol, 99%, ee 97+%

CAS: 1517-69-7 | C8H10O | 122.17 g/mol
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Catalog number L19296.06
also known as L19296-06
Price (USD)
117.65
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Quantity:
5 g
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Price (USD)
117.65
Online Exclusive
131.00
Save 13.35 (10%)
Each
Chemical Identifiers
CAS1517-69-7
IUPAC Name1-phenylethan-1-ol
Molecular FormulaC8H10O
InChI KeyWAPNOHKVXSQRPX-UHFFFAOYNA-N
SMILESCC(O)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥98.5%
Appearance (Color)Clear colorless to pale yellow
Optical Rotation+45° ± 1° (c=5, methanol)
FormLiquid
Enantiomeric excess≥97.0%
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(R)-(+)-1-Phenylethanol is used in the synthesis of optically active products. It is also useful in the determination of enantiomeric purity and for resolutions of acids.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
(R)-(+)-1-Phenylethanol is used in the synthesis of optically active products. It is also useful in the determination of enantiomeric purity and for resolutions of acids.

Solubility
Miscible with organic solvents and slightly miscible with water.

Notes
Incompatible with strong acids and strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Li, Z-J.; Yao, J.; Tao, Q.; Jiang, L.; Lu, T-B. Enantioselective Recognition and Separation of Racemic 1-Phenylethanol by a Pair of 2D Chiral Coordination Polymers. Inorg. Chem. 2013, 52 (20), 11694-11696.
  2. Hosseini-Monfared, H.; Meyer, H.; Janiak, C. Dioxygen oxidation of 1-phenylethanol with gold nanoparticles and N-hydroxyphthalimide in ionic liquid. J. Mol. Catal. A: Chem. 2013, 372, 72-78.