| Identification | More | [Name]
2-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER | [CAS]
118811-03-3 | [Synonyms]
1-BOC-2-(2-HYDROXY-ETHYL)-PIPERIDINE
2-(2-HYDROXYETHYL)-1-BOC-PIPERIDINE
2-(2-HYDROXY-ETHYL)-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
BOC-2-(2-PIPERIDYL)ETHANOL
N-BOC-2-(2-HYDROXYETHYL)PIPERIDINE
N-BOC-2-HYDROXYETHYLPIPERIDINE
N-BOC-2-PIPERIDIN-2-YL-ETHANOL
(+/-)-N-BOC-PIPERIDINE-2-ETHANOL
N-Boc-2-piperidineethanol, 97%
N-Boc-2-(2-hydroxymethyl)piperidine, 2-(2-Hydroxyethyl)piperidine-1-carboxylic acid tert-butyl ester
N-Boc-2-(2-hydroxymethyl)piperidine | [Molecular Formula]
C12H23NO3 | [MDL Number]
MFCD03701252 | [Molecular Weight]
229.32 | [MOL File]
118811-03-3.mol |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
R25:Toxic if swallowed. | [Safety Statements ]
S24/25:Avoid contact with skin and eyes .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 2810 6.1/PG 3 | [WGK Germany ]
3 |
| Hazard Information | Back Directory | [Uses]
Reactant for synthesis of:
- Vasopressin1b receptor antagonists
- CXCR4 antagonists as anti-HIV agents
- Coumarin-based inhibitors of inducible nitric oxide synthase
- Selective thrombin inhibitors
Reactant for:
- N-directed hydroboration for synthesis of amino alcohols
- Enantioselective synthesis of sedamine and allosedamine
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