| Identification | Back Directory | [Name]
1-phenethylpiperidin-4-ol | [CAS]
3518-76-1 | [Synonyms]
1-Phenethyl-4-piperidinol
1-phenethylpiperidin-4-ol
1-(2-Phenylethyl)-4-piperidinol
1-(2-Phenylethyl)piperidin-4-ol
1-(2-Phenylethyl)piperidine-4-ol
4-Piperidinol,1-(2-phenylethyl)-
N-(2-Phenylethyl)-4-hydroxypiperidine
4-Hydroxy-1-(2-phenylethyl)piperidine | [EINECS(EC#)]
222-527-7 | [Molecular Formula]
C13H19NO | [MDL Number]
MFCD00038874 | [MOL File]
3518-76-1.mol | [Molecular Weight]
205.3 |
| Chemical Properties | Back Directory | [Melting point ]
95.5-98.5℃ | [Boiling point ]
341.9±22.0 °C(Predicted) | [density ]
1.064±0.06 g/cm3(Predicted) | [solubility ]
Acetonitrile: Slightly soluble
Chloroform: Soluble
Water: Slightly soluble | [pka]
14.87±0.20(Predicted) |
| Hazard Information | Back Directory | [Uses]
1-Phenethyl-4-piperidinol it is used in preparation of 1-Pyrrolidinyl Indane derivatives as Histamine H3 receptor antagonists useful in treatment of diseases. | [References]
[1] SHANAZ M. TEJANI-BUTT . N-Substituted derivatives of 4-piperidinyl benzilate: Affinities for brain muscarinic acetylcholine receptors[J]. Life sciences, 1990, 47 10: Pages 841-848. DOI: 10.1016/0024-3205(90)90596-j
[2] O. PREZZAVENTO*. Design and Synthesis of New Bifunctional Sigma-1 Selective Ligands with Antioxidant Activity[J]. Journal of Medicinal Chemistry, 2013, 56 6: 2447-2455. DOI: 10.1021/jm3017893
[3] SHIMPEI WATANABE. In Vitro and In Vivo Metabolite Identification Studies for the New Synthetic Opioids Acetylfentanyl, Acrylfentanyl, Furanylfentanyl, and 4-Fluoro-Isobutyrylfentanyl.[J]. AAPS Journal, 2017, 19 4: 1102-1122. DOI: 10.1208/s12248-017-0070-z |
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