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Thermo Scientific Chemicals
(S)-(+)-2-Amino-1-phenylethanol, 97%
CAS: 56613-81-1 | C8H11NO | 137.18 g/mol
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Catalog number L19404.03
also known as L19404-03
Price (USD)
80.65
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89.60Save 8.95 (10%)
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Quantity:
1 g
Price (USD)
80.65
Online Exclusive
89.60Save 8.95 (10%)
Each
Chemical Identifiers
CAS56613-81-1
Specifications
Specification Sheet
Specification SheetFormCrystals or powder or crystalline powder
Melting Point (clear melt)56.0-65.0?C
Appearance (Color)White to pale cream
Optical Rotation42.5 ± 1.0? (C=2 in ethanol)
Assay (GC)≥96.0%
(S)-(+)-2-Amino-1-phenylethanol is used as an intermediate in organic synthesis. It is involved in the preparation of enantiopure (R)-octopamine, (R)-tembamide and (R)-aegeline.
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
(S)-(+)-2-Amino-1-phenylethanol is used as an intermediate in organic synthesis. It is involved in the preparation of enantiopure (R)-octopamine, (R)-tembamide and (R)-aegeline.
Solubility
Soluble in methanol.
Notes
Air sensitive. Incompatible with strong oxidizing agents.
(S)-(+)-2-Amino-1-phenylethanol is used as an intermediate in organic synthesis. It is involved in the preparation of enantiopure (R)-octopamine, (R)-tembamide and (R)-aegeline.
Solubility
Soluble in methanol.
Notes
Air sensitive. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- Zhao, G.; Sun, W.; Wang, J. Purification and characterization of a novel NADPH-dependent 2-aminoacetophenone reductase from Arthrobacter sulfureus. J. Biosci. Bioeng. 2015, 119 (6), 648-651.
- Kourist, R.; Guterl, J. K.; Miyamoto, K.; Sieber, V. Enzymatic Decarboxylation-An Emerging Reaction for Chemicals Production from Renewable Resources. ChemCatChem 2014, 6 (3), 689-701.