(R)-3-Boc-aminopiperidine 309956-78-3

Basic Information:
Chinese name: (R)-3-Boc-aminopiperidine
Chinese alias: alogliptin intermediate 1
R-3-BOC-aminopiperidine
R-3-tert-Butoxycarbonylaminopiperidine
(R)-3-Boc-aminopiperidine
(R)-3-tert-Butoxycarbonylaminopiperidine
-3-(tert-Butoxycarbonyl-amino)-piperidine
(R)-3-N-Boc-aminopiperidine
(R)-N-tert-Butoxycarbonyl-3-aminopiperidine
(R)-3-(N-BOC-amino)piperidine
(R)-3-(N-tert-Butoxycarbonylamino)piperidine
(R)-3-(N-tert-Butoxycarbonyl-amino)-piperidine
(R)-3-BOC-aminopiperidine white crystalline powder
(R)-3-BOC-aminopiperidine, sitagliptin intermediate
(R)-3-BOC-aminopiperidine, an intermediate of alogliptin
English name: (R)-3-(Boc-Amino)piperidine
Alogliptin Intermediate1
(R)-3-Boc-Aminopiperidine
(r)-3-(boc-amio)piperidine
(R)-3-BOC-amino-piperidine
(R)-3-N-Boc-aminopiperidine
(R)-3-(Boc-Amino)piperidine
Linagliptin interMediate B
(R)-3-AMINO-N-TBOC-PIPERIDINE
Alogliptin Benzoate interMediate F
(R)-tert-butyl piperidin-3-ylcarbamate
Tert-Butyl (3R)-Piperidin-3-Ylcarbamate
(R)-TERT-BUTYL-PIPERIDINE-3-YICARBAMATE
(R)-(+)-3-Tert-Butoxycarbonylaminopiperidine
(R)-PIPERIDIN-3-YL-CARBAMIC ACID TERT-BUTYL ESTER
CARBAMIC ACID, (3R)-3-PIPERIDINYL-, 1,1-DIMETHYLETHYL ESTER
Carbamic Acid, N-(3R)-3-Piperidinyl-, 1,1-Dimethylethyl Ester
tert-Butyl[(3R)-piperidin-3-yl]carbamate, (3R)-3-[(tert-Butoxycarbonyl)amino]piperidine
CAS registration number: 309956-78-3
EINECS number: 685-989-2
Molecular formula: C10H20N2O2
Molecular weight: 200.28
 

Physical and chemical properties:
Appearance: white solid 
Melting point: 121.0 to 125.0 °C
Boiling point: 304.8±31.0 °C (Predicted)
Relative density (water = 1): 1.02±0.1 g/cm3 (Predicted)

Quality indicators:
Appearance: white solid
Assay: ≥98%

Additional Information:
Packaging and storage: Keep the container sealed and store in a cool, dry place
Uses: It is an intermediate in organic synthesis and pharmaceutical intermediates, which can be used in laboratory organic synthesis processes and chemical and pharmaceutical research and development processes, as an intermediate for the production of alogliptin and lintagliptin, to synthesize alogliptin benzoate.