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Details

Stereochemistry ACHIRAL
Molecular Formula C7H15NO
Molecular Weight 129.2001
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-PIPERIDINOETHANOL

SMILES

OCCN1CCCCC1

InChI

InChIKey=KZTWONRVIPPDKH-UHFFFAOYSA-N
InChI=1S/C7H15NO/c9-7-6-8-4-2-1-3-5-8/h9H,1-7H2

HIDE SMILES / InChI

Molecular Formula C7H15NO
Molecular Weight 129.2001
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Triarylpyrazoles with basic side chains: development of pyrazole-based estrogen receptor antagonists.
2001 Jan
Indolizino[1,2-b]quinolines derived from A-D rings of camptothecin: synthesis and DNA interaction.
2003 Apr
N-hydroxyethyl-piperidine and -pyrrolidine homoazasugars: preparation and evaluation of glycosidase inhibitory activity.
2003 Jul 31
Stereospecific rearrangements during the synthesis of pyrrolidines and related heterocycles from cyclizations of amino alcohols with vinyl Sulfones.
2003 Nov 28
Studies toward labeling cytisine with [11C]phosgene: rapid synthesis of a delta-lactam involving a new chemoselective lithiation-annulation method.
2004 May 28
Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product.
2005 Aug
The enhancing effect of ion-pairing on the skin permeation of glipizide.
2009
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:24:28 GMT 2023
Edited
by admin
on Fri Dec 15 16:24:28 GMT 2023
Record UNII
VR81F07RX5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-PIPERIDINOETHANOL
Common Name English
NSC-3460
Code English
1-(2-HYDROXYETHYL)PIPERIDINE
Systematic Name English
.BETA.-PIPERIDINOETHANOL
Systematic Name English
1-PIPERIDINEETHANOL
Systematic Name English
N-PIPERIDINEETHANOL
Systematic Name English
Code System Code Type Description
NSC
3460
Created by admin on Fri Dec 15 16:24:28 GMT 2023 , Edited by admin on Fri Dec 15 16:24:28 GMT 2023
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PUBCHEM
18232
Created by admin on Fri Dec 15 16:24:28 GMT 2023 , Edited by admin on Fri Dec 15 16:24:28 GMT 2023
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CHEBI
61238
Created by admin on Fri Dec 15 16:24:28 GMT 2023 , Edited by admin on Fri Dec 15 16:24:28 GMT 2023
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EPA CompTox
DTXSID4062808
Created by admin on Fri Dec 15 16:24:28 GMT 2023 , Edited by admin on Fri Dec 15 16:24:28 GMT 2023
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ECHA (EC/EINECS)
221-244-6
Created by admin on Fri Dec 15 16:24:28 GMT 2023 , Edited by admin on Fri Dec 15 16:24:28 GMT 2023
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CAS
3040-44-6
Created by admin on Fri Dec 15 16:24:28 GMT 2023 , Edited by admin on Fri Dec 15 16:24:28 GMT 2023
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FDA UNII
VR81F07RX5
Created by admin on Fri Dec 15 16:24:28 GMT 2023 , Edited by admin on Fri Dec 15 16:24:28 GMT 2023
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