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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
In vitro cytotoxicity of benzopyranone derivatives with basic side chain against human lung cell lines.
2010-11
Cytotoxic activity and DNA-binding properties of xanthone derivatives.
2010-11
[Study on UV-Vis absorption spectra and fluorescence emission spectra of sixteen tetra-substituted metallophthalocyanine complexes].
2009-05
Analogs of methyl-piperidinopyrazole (MPP): antiestrogens with estrogen receptor alpha selective activity.
2009-01-01
The enhancing effect of ion-pairing on the skin permeation of glipizide.
2009
Synthesis of an optically pure synthetic intermediate of aloperine from a yeast-reductive product.
2005-08
Selective estrogen receptor modulators with conformationally restricted side chains. Synthesis and structure-activity relationship of ERalpha-selective tetrahydroisoquinoline ligands.
2005-01-27
Studies toward labeling cytisine with [11C]phosgene: rapid synthesis of a delta-lactam involving a new chemoselective lithiation-annulation method.
2004-05-28
Stereospecific rearrangements during the synthesis of pyrrolidines and related heterocycles from cyclizations of amino alcohols with vinyl Sulfones.
2003-11-28
Synthesis of sparteine-like chiral diamines and evaluation in the enantioselective lithiation-substitution of N-(tert-butoxycarbonyl)pyrrolidine.
2003-11-21
N-hydroxyethyl-piperidine and -pyrrolidine homoazasugars: preparation and evaluation of glycosidase inhibitory activity.
2003-07-31
Indolizino[1,2-b]quinolines derived from A-D rings of camptothecin: synthesis and DNA interaction.
2003-04
Formaldehyde-induced DNA cross-link of indolizino[1,2-b]quinolines derived from the A-D rings of camptothecin.
2002-12-19
Triarylpyrazoles with basic side chains: development of pyrazole-based estrogen receptor antagonists.
2001-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:27:05 GMT 2025
Edited
by admin
on Mon Mar 31 18:27:05 GMT 2025
Record UNII
VR81F07RX5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-PIPERIDINOETHANOL
Common Name English
NSC-3460
Preferred Name 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 Mon Mar 31 18:27:05 GMT 2025 , Edited by admin on Mon Mar 31 18:27:05 GMT 2025
PRIMARY
PUBCHEM
18232
Created by admin on Mon Mar 31 18:27:05 GMT 2025 , Edited by admin on Mon Mar 31 18:27:05 GMT 2025
PRIMARY
CHEBI
61238
Created by admin on Mon Mar 31 18:27:05 GMT 2025 , Edited by admin on Mon Mar 31 18:27:05 GMT 2025
PRIMARY
EPA CompTox
DTXSID4062808
Created by admin on Mon Mar 31 18:27:05 GMT 2025 , Edited by admin on Mon Mar 31 18:27:05 GMT 2025
PRIMARY
ECHA (EC/EINECS)
221-244-6
Created by admin on Mon Mar 31 18:27:05 GMT 2025 , Edited by admin on Mon Mar 31 18:27:05 GMT 2025
PRIMARY
CAS
3040-44-6
Created by admin on Mon Mar 31 18:27:05 GMT 2025 , Edited by admin on Mon Mar 31 18:27:05 GMT 2025
PRIMARY
FDA UNII
VR81F07RX5
Created by admin on Mon Mar 31 18:27:05 GMT 2025 , Edited by admin on Mon Mar 31 18:27:05 GMT 2025
PRIMARY