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ChemicalBook--->CAS DataBase List--->89151-44-0

89151-44-0

89151-44-0 Structure

89151-44-0 Structure
IdentificationMore
[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 PropertiesBack 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
[pka]

15.10±0.10(Predicted)
[CAS DataBase Reference]

89151-44-0(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[WGK Germany ]

3
[HS Code ]

2933399990
Hazard InformationBack 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.
Spectrum DetailBack Directory
[Spectrum Detail]

1-Boc-4-(2-hydroxyethyl)piperidine(89151-44-0)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

89151-44-0(sigmaaldrich)
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