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Details

Stereochemistry ACHIRAL
Molecular Formula C7H15N
Molecular Weight 113.2007
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-ETHYLPIPERIDINE

SMILES

CCN1CCCCC1

InChI

InChIKey=HTLZVHNRZJPSMI-UHFFFAOYSA-N
InChI=1S/C7H15N/c1-2-8-6-4-3-5-7-8/h2-7H2,1H3

HIDE SMILES / InChI

Molecular Formula C7H15N
Molecular Weight 113.2007
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Binary complexes of tertiary amines with phenylacetylene. Dispersion wins over electrostatics.
2010-06-21
Design, synthesis, evaluation and QSAR analysis of N(1)-substituted norcymserine derivatives as selective butyrylcholinesterase inhibitors.
2010-03-01
Chemometrical study of the anaesthetical activity of alkoxyphenylcarbamic acid esters.
2010-03
Effects of DNA threading bis(9-aminoacridine-4-carboxamides) on global gene expression.
2010-01-13
Partial phenotypic reversion of ABA-deficient flacca tomato (Solanum lycopersicum) scions by a wild-type rootstock: normalizing shoot ethylene relations promotes leaf area but does not diminish whole plant transpiration rate.
2009
DNA threading bis(9-aminoacridine-4-carboxamides): effects of piperidine sidechains on DNA binding, cytotoxicity and cell cycle arrest.
2008-04-15
Room temperature phosphorescence of alpha-bromonaphthalene induced by cyclodextrin in the presence of hexahydropyridine or 1-ethylpiperidine and its application.
2007-02-05
Inhibition of lipase activities by basic polysaccharide.
2007-02
Synthesis of 2',3'-dideoxyinosine via radical deoxygenation.
2007
Novel phosphorus radical-based routes to horsfiline.
2005-07-21
Investigations on the effects of basic side chains on the hormonal profile of (4R,5S)/(4S,5R)-4,5-bis(4-hydroxyphenyl)-2-imidazolines.
2005-01-27
11H-Isoquino[4,3-c]cinnolin-12-ones; novel anticancer agents with potent topoisomerase I-targeting activity and cytotoxicity.
2004-02-15
Diethylphosphine oxide (DEPO): high-yielding and facile preparation of indolones in water.
2003-08-07
Stereoselective synthesis of tetrasubstituted (Z)-alkenes from aryl alkyl ketones utilizing the Horner-Wadsworth-Emmons reaction.
2002-09
Synthesis and structural studies of 1,1'-bis-amino-functionalized ferrocenes, ferrocene salts, and ferrocenium salts.
2002-02-25
Design, synthesis and biological evaluation of a novel series of potent, orally active adenosine A1 receptor antagonists with high blood-brain barrier permeability.
2001-08
A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water.
2001-04-19
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 19:00:24 GMT 2025
Edited
by admin
on Mon Mar 31 19:00:24 GMT 2025
Record UNII
7IE43L0926
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-2090
Preferred Name English
N-ETHYLPIPERIDINE
Systematic Name English
1-ETHYLPIPERIDINE
Systematic Name English
PIPERIDINE, 1-ETHYL-
Systematic Name English
Code System Code Type Description
MESH
C430119
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY
NSC
2090
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY
FDA UNII
7IE43L0926
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY
CHEBI
39017
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY
CAS
766-09-6
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY
PUBCHEM
13007
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY
EPA CompTox
DTXSID1061102
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY
ECHA (EC/EINECS)
212-161-6
Created by admin on Mon Mar 31 19:00:24 GMT 2025 , Edited by admin on Mon Mar 31 19:00:24 GMT 2025
PRIMARY