Identification | More | [Name]
(S)-2-Phenyl-1-propylamine | [CAS]
17596-79-1 | [Synonyms]
(S)-(-)-2-PHENYL-1-PROPYLAMINE (S)-2-PHENYL-1-PROPYLAMINE (S)-2-PHENYLPROPYLAMINE (S)-(-)-BETA-METHYLPHENETHYLAMINE (S)-BETA-METHYLPHENETHYLAMINE S(-)-beta-methylphenylethylamine (S)-(-)-β-Methylphenethylamine (S)-(-)-Beta-Methlphenethylamine (S)-2-Phenylpropylamine(S)-(-)-b-Methylphenethylamine (S)-2-PHENYL-1-PROPYLAMINE 99+% (2s)-2-phenylpropan-1-amine S-(-)-β-METHYLPHENETHYLAMINE (S-(-)-2-PHENYLPROPYLAMINE) | [Molecular Formula]
C9H13N | [MDL Number]
MFCD00216741 | [Molecular Weight]
135.21 | [MOL File]
17596-79-1.mol |
Chemical Properties | Back Directory | [Melting point ]
207 °C(lit.) | [alpha ]
-35 º (c=1, EtOH) | [Boiling point ]
208.93°C (estimate) | [density ]
0.945 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.525(lit.)
| [Fp ]
178 °F
| [pka]
9.92±0.10(Predicted) | [optical activity]
[α]22/D 35°, c = 1 in ethanol | [BRN ]
3195645 | [CAS DataBase Reference]
17596-79-1(CAS DataBase Reference) |
Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . S27:Take off immediately all contaminated clothing . | [RIDADR ]
UN 2735 8/PG 3
| [WGK Germany ]
3
| [F ]
10-34 | [HS Code ]
29214990 |
Hazard Information | Back Directory | [Uses]
(s)-2-Phenyl-1-propanamine is a preparation of the pyrazolyl containing tricyclic derivative and their application as anticancer agents. | [Uses]
Building block for the enantioselective synthesis of pyrizinostatin, a pyroglutamyl peptidase inhibitor. | [General Description]
Bacteriorhodopsin is the prototypical "seven-helix" transmembrane protein (with seven α-helical domains), whose study led to advances in understanding G protein-coupled receptors (GPCRs). In Halobacteria, it acts as a light-harvesting protein, producing a proton gradient across the cell wall that is then used to drive biosynthetic processes. |
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