1-Phenylethylamine[1] | |
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1-phenylethan-1-amine |
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Other names
(±)-1-Phenylethylamine, (±)-α-Methylbenzylamine |
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Identifiers | |
CAS number | 618-36-0 |
ChemSpider | 7130 |
KEGG | C02455 |
ChEBI | CHEBI:670 |
ChEMBL | CHEMBL278059 |
Jmol-3D images | Image 1 Image 2 |
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Properties | |
Molecular formula | C6H5CH(CH3)NH2 |
Molar mass | 121.18 g/mol |
Density | 0.94 g/ml at 25 °C |
Boiling point |
185 °C |
Hazards | |
Main hazards | Corrosive |
Related compounds | |
Related stereoisomers | (R)-(+)- (CAS [3886-69-9]) (S)-(–)- (CAS [2627-86-3]) |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
1-Phenylethylamine is a monoamine compound. Individual enantiomers of this basic compound are useful for performing chiral resolution of acidic compounds by forming diastereomeric salts.
This compound may be prepared by the reductive amination of acetophenone under various standard conditions for this type of reaction. One major route for this chemical uses the Mignonac reaction, a one-pot protocol using hydrogen gas as the reducing agent:[2]