Identification | More | [Name]
1-Boc-4-(2-hydroxyethyl)piperidine | [CAS]
89151-44-0 | [Synonyms]
1-BOC-4-(2-HYDROXYETHYL)PIPERIDINE 4-(2-HYDROXYETHYL)PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER BOC-2-(4-PIPERIDYL)ETHANOL N-BOC-4-PIPERIDINEETHANOL N-(TERT-BUTOXYCARBONYL)-4-PIPERIDINEETHANOL 4-(2-Hydroxyethyl)piperidine, N-BOC protected 1-BOC-4-PIPERIDINE EHTANOL 1-PIPERIDINECARBOXYLIC ACID, 4-(2-HYDROXYETHYL)-1, N-TERT-BUTOXYCARBONYL-4-PIPERIDINEETHANOL 95+% tert-butyl 4-(2-hydroxyethyl)piperidine-1-carboxylate | [EINECS(EC#)]
692-472-5 | [Molecular Formula]
C12H23NO3 | [MDL Number]
MFCD03427086 | [Molecular Weight]
229.32 | [MOL File]
89151-44-0.mol |
Chemical Properties | Back Directory | [Boiling point ]
120-150 °C/0.5 mmHg (lit.) | [density ]
1.043 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.4730(lit.)
| [Fp ]
>230 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
viscous liquid | [pka]
15.10±0.10(Predicted) | [color ]
Colourless to light yellow | [CAS DataBase Reference]
89151-44-0(CAS DataBase Reference) |
Hazard Information | Back Directory | [Uses]
N-BOC-4-piperidine-β-ethanol is used to prepare anilinoquinazoline VEGF receptor tyrosine kinase inhibitors with antitumor activities. It is also used to synthesize 1,3,4-trisubstituted pyrrolidine CCR5 receptor antagonists with antiviral activities. |
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