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Thermo Scientific™
D-Phenylalaninol, 98%, Thermo Scientific Chemicals
| Catalog Number | Quantity |
|---|---|
| L09697.03 also known as L09697-03 | 1 g |
Chemical Identifiers
CAS5267-64-1
IUPAC Name2-amino-3-phenylpropan-1-ol
Molecular FormulaC9H13NO
InChI KeySTVVMTBJNDTZBF-UHFFFAOYNA-N
SMILESNC(CO)CC1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale yellow
Assay (Non-aqueous acid-base Titration)>97.5%
Formcrystalline powder
Optical Rotation+23 ? 2? (c=5 in ethanol)
D-Phenylalaninol is used as a chiral auxiliary for asymmetric Michael reactions. It is an enantiomer of L-Phenylalaninol, an inhibitor of intestinal Phenylalanine absorption. It acts as an inhibiting agent to the enzymes which are responsible for the breakdown of endorphins.
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
D-Phenylalaninol is used as a chiral auxiliary for asymmetric Michael reactions. It is an enantiomer of L-Phenylalaninol, an inhibitor of intestinal Phenylalanine absorption. It acts as an inhibiting agent to the enzymes which are responsible for the breakdown of endorphins.
Solubility
Soluble in Dichloromethane, Ethyl Acetate, Methanol.
Notes
Air Sensitive. Store away from air. Store under dry inert gas. Incompatible with carbondioxide, air, acids and oxidizing agents.
D-Phenylalaninol is used as a chiral auxiliary for asymmetric Michael reactions. It is an enantiomer of L-Phenylalaninol, an inhibitor of intestinal Phenylalanine absorption. It acts as an inhibiting agent to the enzymes which are responsible for the breakdown of endorphins.
Solubility
Soluble in Dichloromethane, Ethyl Acetate, Methanol.
Notes
Air Sensitive. Store away from air. Store under dry inert gas. Incompatible with carbondioxide, air, acids and oxidizing agents.
RUO – Research Use Only
General References:
- W W Mak; J T Wong. Relationship between membrane fluidity and capping of receptors for concanavalin A.Canadian journal of biochemistry.1980, 58 (12), 1421-1429.
- W W Mak; L Pinteric; J T Wong. Enhanced sensitivity of tumorigenic cells to rapid rounding induced by phenylalaninol.Canadian journal of biochemistry.1980, 58 (9), 737-744.
- Has been used as a chiral auxiliary for asymmetric Michael reactions: J. Org. Chem., 50, 3863 (1985).