| Identification | More | [Name]
(R)-1-Boc-3-Hydroxypiperidine | [CAS]
143900-43-0 | [Synonyms]
1-PIPERIDINECARBOXYLIC ACID, 3-HYDROXY-, 1,1-DIMETHYLETHYL ESTER, (3R)-
(R)-1-BOC-3-HYDROXYPIPERIDINE
(R)-1-BOC-3-PIPERIDINOL
(R)-1-N-BOC-3-HYDROXYPIPERIDINE
R-3-HYDROXY-1-(TERT-BUTOXYCARBONYL)PIPERIDINE
(R)-3-HYDROXY-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
(R)-N-BOC-3-HYDROXYPIPERIDINE
(R)-N-(TERT-BUTOXYCARBONYL)-3-HYDROXYPIPERIDINE HYDROCHLORIDE
(R)-TERT BUTYL-3-HYDROXYPIPERIDINE-1-CARBOXYLATE
(R)-1-TERT-BUTOXYCARBONYL-3-AMINOPIPERIDINE
(R)-3-Hydroxypiperidine, N-BOC protected | [Molecular Formula]
C10H19NO3 | [MDL Number]
MFCD06659042 | [Molecular Weight]
201.26 | [MOL File]
143900-43-0.mol |
| Chemical Properties | Back Directory | [Melting point ]
43-50 °C | [Boiling point ]
292.3±33.0 °C(Predicted) | [density ]
1.107±0.06 g/cm3(Predicted) | [Fp ]
104°C | [storage temp. ]
2-8°C | [solubility ]
soluble in Methanol | [form ]
Low Melting Solid | [pka]
14.74±0.20(Predicted) | [color ]
White to tan | [optical activity]
[α]/D 22±3°, c = 5 in methanol | [InChIKey]
UIJXHKXIOCDSEB-MRVPVSSYSA-N | [CAS DataBase Reference]
143900-43-0(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R41:Risk of serious damage to eyes.
R37/38:Irritating to respiratory system and skin .
R25:Toxic if swallowed. | [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) . | [RIDADR ]
UN 2811 6.1/PG 3 | [WGK Germany ]
3 | [HazardClass ]
6.1 | [PackingGroup ]
Ⅲ | [HS Code ]
29333990 |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
(R)-1-Boc-3-hydroxypiperidine has been used as a reactant for the synthesis of piperidinyl and pyrrolidinyl butyrates. It has also been used for the synthesis of constrained (-)-S-adenosyl-L-homocysteine (SAH) analogs as DNA methyltransferase inhibitors. |
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