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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H20N2O2
Molecular Weight 200.278
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-(Boc-amino)piperidine, (R)-

SMILES

CC(C)(C)OC(=O)N[C@@H]1CCCNC1

InChI

InChIKey=WUOQXNWMYLFAHT-MRVPVSSYSA-N
InChI=1S/C10H20N2O2/c1-10(2,3)14-9(13)12-8-5-4-6-11-7-8/h8,11H,4-7H2,1-3H3,(H,12,13)/t8-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H20N2O2
Molecular Weight 200.278
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 17:45:02 GMT 2025
Edited
by admin
on Wed Apr 02 17:45:02 GMT 2025
Record UNII
YXS4RFE6R8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(R)-3-Boc-aminopiperidine
Preferred Name English
3-(Boc-amino)piperidine, (R)-
Common Name English
1,1-Dimethylethyl N-(3R)-3-piperidinylcarbamate
Systematic Name English
(R)-3-(Boc-amino)piperidine
Systematic Name English
(3R)-3-[((tert-Butyloxycarbonyl)amino)]piperidine
Systematic Name English
(R)-3-(tert-Butoxycarbonylamino)piperidine
Systematic Name English
Carbamic acid, (3R)-3-piperidinyl-, 1,1-dimethylethyl ester
Systematic Name English
(R)-3-(N-Boc-amino)piperidine
Systematic Name English
(R)-3-[(tert-Butyloxycarbonyl)amino]piperidine
Systematic Name English
(R)-3-[(tert-Butoxycarbonyl)amino]piperidine
Systematic Name English
Carbamic acid, N-(3R)-3-piperidinyl-, 1,1-dimethylethyl ester
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID30363796
Created by admin on Wed Apr 02 17:45:02 GMT 2025 , Edited by admin on Wed Apr 02 17:45:02 GMT 2025
PRIMARY
PUBCHEM
1514172
Created by admin on Wed Apr 02 17:45:02 GMT 2025 , Edited by admin on Wed Apr 02 17:45:02 GMT 2025
PRIMARY
FDA UNII
YXS4RFE6R8
Created by admin on Wed Apr 02 17:45:02 GMT 2025 , Edited by admin on Wed Apr 02 17:45:02 GMT 2025
PRIMARY
CAS
309956-78-3
Created by admin on Wed Apr 02 17:45:02 GMT 2025 , Edited by admin on Wed Apr 02 17:45:02 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
SALT/SOLVATE -> PARENT