N-METHYLPIPERIDINE-2-ETHANOL CAS#: 533-15-3; ChemWhat Code: 782414

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product NameN-METHYLPIPERIDINE-2-ETHANOL
IUPAC Name2-(1-methylpiperidin-2-yl)ethanol
Molecular StructureStructure of N-Methylpiperidine-2-Ethanol CAS 533-15-3
CAS Registry Number 533-15-3
MDL NumberMFCD00673141
Synonyms2-(1-methylpiperidin-2-yl)ethanol
533-15-3
2-Piperidineethanol, 1-methyl-
1-Methylpiperidine-2-ethanol
N-METHYLPIPERIDINE-2-ETHANOL
EINECS 208-554-7
NSC 75616
DTXSID90862134
lobelol
MFCD00673141
SCHEMBL803674
DTXCID80810942
OVMRRCXDBKEQIU-UHFFFAOYSA-N
NSC75616
NSC-75616
STK499941
AKOS005171386
SB41849
2-(1-methylpiperidin-2-yl)ethan-1-ol
DS-022273
NS00042977
EN300-62687
G70683
Z139565496
208-554-7
Molecular FormulaC8H17NO
Molecular Weight143.23
InChIInChI=1S/C8H17NO/c1-9-6-3-2-4-8(9)5-7-10/h8,10H,2-7H2,1H3 
InChI KeyOVMRRCXDBKEQIU-UHFFFAOYSA-N
Canonical SMILESCN1CCCCC1CCO

Physical Data

AppearanceWhite powder
Boiling Point, °CPressure (Boiling Point), Torr
750.9
72 – 730.5
105 – 10711
105 – 107105 – 107
65 – 680.1 – 0.3
77 – 790.7
802
Density, g·cm-3Reference Temperature, °CMeasurement Temperature, °C
0.984420
0.989240
0.977417.5

Spectra

Description (NMR Spectroscopy)
Chemical shifts, Spectrum

Route of Synthesis (ROS)

Route of Synthesis (ROS) of N-Methylpiperidine-2-Ethanol CAS 533-15-3
Route of Synthesis (ROS) of N-Methylpiperidine-2-Ethanol CAS 533-15-3
ConditionsYield
With lithium aluminium tetrahydride In tetrahydrofuran at 60℃;

Experimental Procedure
Step 2: Synthesis of 2-(1-methylpiperidin-2-yl)ethan-1-ol (B15-2-3)
Add 2-(2-hydroxyethyl)piperidine-1-carboxylate tert-butyl ester (3.4g, 15mmol) in the reaction flask, add 24mLTHF, then add LiAlH4 (3.3g, 89mmol), reflux and stir at 60°C 4h, TLC was used to detect the progress of the reaction. When the reaction was complete, the reaction was quenched by pouring ice water at low temperature. The resulting suspension was filtered with diatomaceous earth. The filtrate was extracted with dichloromethane/water system, the organic phases were combined, and the organic phase was washed with water and brine once, and the organic phase was dried with anhydrous sodium sulfate, concentrated in vacuo, and purified with a silica gel column to obtain the compound intermediate 2-(1-methyl piperidin-2-yl)ethan-1-ol (1.5 g, 71.4%).
71.4 %
With lithium aluminium tetrahydride In tetrahydrofuran at 60℃;

Experimental Procedure

Step 2: Synthesis of 2-(1-methylpiperidin-2-yl)ethan-1-ol (B15-2-3)
Add 2-(2-hydroxyethyl)piperidine-1-carboxylate tert-butyl ester (3.4g, 15mmol) in the reaction flask, add 24mLTHF, then add LiAlH4 (3.3g, 89mmol), reflux and stir at 60°C 4h, TLC was used to detect the progress of the reaction. When the reaction was complete, the reaction was quenched by pouring ice water at low temperature. The resulting suspension was filtered with diatomaceous earth. The filtrate was extracted with dichloromethane/water system, the organic phases were combined, and the organic phase was washed with water and brine once, and the organic phase was dried with anhydrous sodium sulfate, concentrated in vacuo, and purified with a silica gel column to obtain the compound intermediate 2-(1-methyl piperidin-2-yl)ethan-1-ol (1.5 g, 71.4%).
71.4 %

Safety and Hazards

GHS Hazard StatementsNot Classified

Source: European Chemicals Agency (ECHA)
License Note: Use of the information, documents and data from the ECHA website is subject to the terms and conditions of this Legal Notice, and subject to other binding limitations provided for under applicable law, the information, documents and data made available on the ECHA website may be reproduced, distributed and/or used, totally or in part, for non-commercial purposes provided that ECHA is acknowledged as the source: “Source: European Chemicals Agency, http://echa.europa.eu/”. Such acknowledgement must be included in each copy of the material. ECHA permits and encourages organisations and individuals to create links to the ECHA website under the following cumulative conditions: Links can only be made to webpages that provide a link to the Legal Notice page.
License URL: https://echa.europa.eu/web/guest/legal-notice
Record Name: (1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphate
URL: https://echa.europa.eu/information-on-chemicals/cl-inventory-database/-/discli/details/213446
Description: The information provided here is aggregated from the “Notified classification and labelling” from ECHA’s C&L Inventory. Read more: https://echa.europa.eu/information-on-chemicals/cl-inventory-database


Other Data

TransportationUnder room temperature away from light
StorageUnder room temperature away from light
Shelf Life2 years
Market Price
Druglikeness
Lipinski rules component
Molecular Weight143.229
logP0.613
HBA2
HBD1
Matching Lipinski Rules4
Veber rules component
Polar Surface Area (PSA)23.47
Rotatable Bond (RotB)2
Matching Veber Rules2
Use Pattern
N-METHYLPIPERIDINE-2-ETHANOL CAS#: 533-15-3 3-Aminopyridine CAS#: 462-08-8 commonly used in pharmaceutical intermediates.

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