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Details

Stereochemistry ACHIRAL
Molecular Formula C7H9N
Molecular Weight 107.1531
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-ETHYLPYRIDINE

SMILES

CCC1=NC=CC=C1

InChI

InChIKey=NRGGMCIBEHEAIL-UHFFFAOYSA-N
InChI=1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C7H9N
Molecular Weight 107.1531
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dicopper(I) complexes of unsymmetrical binucleating ligands and their dioxygen reactivities.
2001 Feb 12
Identification of distinctive volatile compounds in fish sauce.
2002 Sep 11
Ligand effect on reversible conversion between copper(I) and bis(mu-oxo)dicopper(III) complex with a sterically hindered tetradentate tripodal ligand and monooxygenase activity of bis(mu-oxo)dicopper(III) complex.
2003 Dec 15
Thermochemical study of the ethylpyridine and ethylpyrazine isomers.
2003 Dec 7
Pyridines in cigarette smoke inhibit hamster oviductal functioning in picomolar doses.
2003 Mar-Apr
Quantitation of isomeric ethyl pyridine mixtures by multivariate calibration applied to ion-molecule reaction/collision-induced dissociation triple-stage mass spectra.
2003 May 28
Nickel(II) cyclidenes with appended ethylpyridine receptor centers as molecular tweezers for dicarboxylic acids.
2003 Oct 20
Synthesis and structure-activity relationships of thieno[2,3-d]pyrimidine-2,4-dione derivatives as potent GnRH receptor antagonists.
2003 Oct 20
Aromatic vs aliphatic C-H cleavage of alkyl-substituted pyridines by (PNPiPr)Re compounds.
2004 Feb 25
Synthesis and structure-activity relationships of 1-arylmethyl-5-aryl-6-methyluracils as potent gonadotropin-releasing hormone receptor antagonists.
2004 Feb 26
Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning.
2004 May 12
Synthesis of chiral nonracemic 1-(2-pyridinyl)ethylamines: stereospecific introduction of amino function onto the 2-pyridinylmethyl carbon center.
2004 Oct 1
Identification of components responsible for the odor of cigar smoker's breath.
2006 Jan 25
Cigarette smoke toxicants alter growth and survival of cultured mammalian cells.
2006 Sep
Opioid ligands with mixed properties from substituted enantiomeric N-phenethyl-5-phenylmorphans. Synthesis of a micro-agonist delta-antagonist and delta-inverse agonists.
2007 Apr 21
Smoke from traditional commercial, harm reduction and research brand cigarettes impairs oviductal functioning in hamsters (Mesocricetus auratus) in vitro.
2007 Feb
Generation of pyridyl coordinated organosilicon cation pool by oxidative Si-Si bond dissociation.
2007 Feb 8
Alkylation effects on strong collisions of highly vibrationally excited alkylated pyridines with CO2.
2007 May 17
Understanding the formation of N-H tautomers from alpha-substituted pyridines: tautomerization of 2-ethylpyridine promoted by osmium.
2007 Sep 12
Pharmaceutical analysis by supercritical fluid chromatography: Optimization of the mobile phase composition on a 2-ethylpyridine column.
2008 May
Prediction of retention for sulfonamides in supercritical fluid chromatography.
2008 May 2
2,6-Bis[1-(2,6-diethyl-phenyl-imino)eth-yl]pyridine.
2008 Nov 20
Diaqua-sodium(I) perchlorate bis-[μ-2-(carboxyl-atomethyl-imino-meth-yl)phenolato]bis-[(3-methyl-pyridine)copper(II)].
2008 Nov 29
Improved separation of furocoumarins of essential oils by supercritical fluid chromatography.
2009 Oct 16
Effect of increasing concentration of ammonium acetate as an additive in supercritical fluid chromatography using CO2-methanol mobile phase.
2009 Sep 4
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 20:25:57 GMT 2023
Edited
by admin
on Fri Dec 15 20:25:57 GMT 2023
Record UNII
06X1W46PYX
Record Status Validated (UNII)
Record Version
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Name Type Language
2-ETHYLPYRIDINE
Systematic Name English
.ALPHA.-ETHYLPYRIDINE
Systematic Name English
PYRIDINE, ETHYL-
Systematic Name English
NSC-964
Code English
PYRIDINE, 2-ETHYL-
Systematic Name English
Code System Code Type Description
CAS
28631-77-8
Created by admin on Fri Dec 15 20:25:57 GMT 2023 , Edited by admin on Fri Dec 15 20:25:57 GMT 2023
NON-SPECIFIC SUBSTITUTION
FDA UNII
06X1W46PYX
Created by admin on Fri Dec 15 20:25:57 GMT 2023 , Edited by admin on Fri Dec 15 20:25:57 GMT 2023
PRIMARY
PUBCHEM
7523
Created by admin on Fri Dec 15 20:25:57 GMT 2023 , Edited by admin on Fri Dec 15 20:25:57 GMT 2023
PRIMARY
EPA CompTox
DTXSID4021844
Created by admin on Fri Dec 15 20:25:57 GMT 2023 , Edited by admin on Fri Dec 15 20:25:57 GMT 2023
PRIMARY
CAS
100-71-0
Created by admin on Fri Dec 15 20:25:57 GMT 2023 , Edited by admin on Fri Dec 15 20:25:57 GMT 2023
PRIMARY
NSC
964
Created by admin on Fri Dec 15 20:25:57 GMT 2023 , Edited by admin on Fri Dec 15 20:25:57 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-881-9
Created by admin on Fri Dec 15 20:25:57 GMT 2023 , Edited by admin on Fri Dec 15 20:25:57 GMT 2023
PRIMARY