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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 4-ETHYLPYRIDINE

SMILES

CCC1=CC=NC=C1

InChI

InChIKey=VJXRKZJMGVSXPX-UHFFFAOYSA-N
InChI=1S/C7H9N/c1-2-7-3-5-8-6-4-7/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
Synthesis and structural and magnetic characterisation of cobalt(ii) complexes of mixed phosphonate-antimonate ligands.
2010-10-28
Ultrafast excited-state dynamics of [Re(L)(CO)3(bpy)]n complexes: involvement of the solvent.
2010-06-10
New discrete and polymeric supramolecular architectures derived from dinuclear Co(II), Ni(II) and Cu(II) complexes of aryl-linked bis-beta-diketonato ligands and nitrogen bases: synthetic, structural and high pressure studies.
2010-03-21
Control of the photoreactivity of diarylethene derivatives by quaternarization of the pyridylethynyl group.
2008-05-15
Synthetic, structural, electrochemical and solvent extraction studies of neutral trinuclear Co(II), Ni(II), Cu(II) and Zn(II) metallocycles and tetrahedral tetranuclear Fe(III) species incorporating 1,4-aryl-linked bis-beta-diketonato ligands.
2008-03-14
Octahedral adducts of dichlorosilane with substituted pyridines: synthesis, reactivity and a comparison of their structures and (29)si NMR chemical shifts.
2008
Neutral (bis-beta-diketonato) iron(III), cobalt(II), nickel(II), copper(II) and zinc(II) metallocycles: structural, electrochemical and solvent extraction studies.
2007-05-07
Synthesis, characterization, and preliminary oxygenation studies of benzyl- and ethyl-substituted pyridine ligands of carboxylate-rich diiron(II) complexes.
2006-01-23
Aerobic biodegradation of 4-methylpyridine and 4-ethylpyridine by newly isolated Pseudonocardia sp. strain M43.
2006-01
Simple chip-based interfaces for on-line monitoring of supramolecular interactions by nano-ESI MS.
2005-10
Synthesis of chiral nonracemic 1-(2-pyridinyl)ethylamines: stereospecific introduction of amino function onto the 2-pyridinylmethyl carbon center.
2004-10-01
Excited-state dynamics of fac-[ReI(L)(CO)3(phen)]+ and fac-[ReI(L)(CO)3(5-NO2-phen)]+ (L = imidazole, 4-ethylpyridine; phen = 1,10-phenanthroline) complexes.
2004-08-09
Thermochemical study of the ethylpyridine and ethylpyrazine isomers.
2003-12-07
Application of time-resolved infrared spectroscopy to electronic structure in metal-to-ligand charge-transfer excited states.
2002-11-18
Direct sampling tandem mass spectrometry (MS/MS) and multiway calibration for isomer quantitation.
2002-08
Normal coordinate analysis of 4-aminopyridine. Effect of substituent on pyridine ring in metal complexes of 4-substituted pyridines.
2001-06
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:37:52 GMT 2025
Edited
by admin
on Mon Mar 31 19:37:52 GMT 2025
Record UNII
3KW0SE2TL5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-822
Preferred Name English
4-ETHYLPYRIDINE
MI  
Systematic Name English
4-ETHYLPYRIDINE [MI]
Common Name English
.GAMMA.-ETHYLPYRIDINE
Common Name English
PYRIDINE, 4-ETHYL-
Systematic Name English
Code System Code Type Description
SMS_ID
300000053033
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY
FDA UNII
3KW0SE2TL5
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY
NSC
822
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY
CAS
536-75-4
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-646-7
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY
EPA CompTox
DTXSID60873555
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY
MERCK INDEX
m5171
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY Merck Index
PUBCHEM
10822
Created by admin on Mon Mar 31 19:37:52 GMT 2025 , Edited by admin on Mon Mar 31 19:37:52 GMT 2025
PRIMARY