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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
A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water.
2001 Apr 19
Design, synthesis and biological evaluation of a novel series of potent, orally active adenosine A1 receptor antagonists with high blood-brain barrier permeability.
2001 Aug
Triarylpyrazoles with basic side chains: development of pyrazole-based estrogen receptor antagonists.
2001 Jan
Synthesis and structural studies of 1,1'-bis-amino-functionalized ferrocenes, ferrocene salts, and ferrocenium salts.
2002 Feb 25
Stereoselective synthesis of tetrasubstituted (Z)-alkenes from aryl alkyl ketones utilizing the Horner-Wadsworth-Emmons reaction.
2002 Sep
Diethylphosphine oxide (DEPO): high-yielding and facile preparation of indolones in water.
2003 Aug 7
11H-Isoquino[4,3-c]cinnolin-12-ones; novel anticancer agents with potent topoisomerase I-targeting activity and cytotoxicity.
2004 Feb 15
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 Jan 27
Novel phosphorus radical-based routes to horsfiline.
2005 Jul 21
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
Binary complexes of tertiary amines with phenylacetylene. Dispersion wins over electrostatics.
2010 Jun 21
Chemometrical study of the anaesthetical activity of alkoxyphenylcarbamic acid esters.
2010 Mar
Design, synthesis, evaluation and QSAR analysis of N(1)-substituted norcymserine derivatives as selective butyrylcholinesterase inhibitors.
2010 Mar 1
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:00:36 GMT 2023
Edited
by admin
on Fri Dec 15 18:00:36 GMT 2023
Record UNII
7IE43L0926
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-ETHYLPIPERIDINE
Systematic Name English
1-ETHYLPIPERIDINE
Systematic Name English
PIPERIDINE, 1-ETHYL-
Systematic Name English
NSC-2090
Code English
Code System Code Type Description
MESH
C430119
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY
NSC
2090
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY
FDA UNII
7IE43L0926
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY
CHEBI
39017
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY
CAS
766-09-6
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY
PUBCHEM
13007
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID1061102
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY
ECHA (EC/EINECS)
212-161-6
Created by admin on Fri Dec 15 18:00:36 GMT 2023 , Edited by admin on Fri Dec 15 18:00:36 GMT 2023
PRIMARY