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Details

Stereochemistry ACHIRAL
Molecular Formula C8H11N
Molecular Weight 121.1796
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYLANILINE

SMILES

CCNC1=CC=CC=C1

InChI

InChIKey=OJGMBLNIHDZDGS-UHFFFAOYSA-N
InChI=1S/C8H11N/c1-2-9-8-6-4-3-5-7-8/h3-7,9H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C8H11N
Molecular Weight 121.1796
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 situ STM study of the adsorption and electropolymerization of o-, m-, and p-ethylaniline molecules on Au(111) electrode.
2010-08-28
4-Ethyl-anilinium perchlorate-18-crown-6 (1/1).
2010-08-11
(R)-1-Phenyl-ethyl-ammonium trifluoro-acetate.
2010-04-21
Prevalence and molecular characterization of Cryptosporidium spp. in dairy cattle in South Bohemia, the Czech Republic.
2009-10-28
Cryptosporidium pig genotype II in immunocompetent man.
2009-06
(S,R,Rp)-N,N-Dimethyl-1-{2-[(1-phenyl-ethyl)amino-meth-yl]ferrocen-yl}ethanamine.
2009-03-25
Molecular characterization of Cryptosporidium isolates from pigs at slaughterhouses in South Bohemia, Czech Republic.
2009-01
Sensory properties and color measurements of dietary chocolates with different compositions during storage for up to 360 days.
2009
4-(4-Ethyl-phenyl-diazen-yl)phenol.
2008-05-10
Spectroscopic studies of molecular interactions involving 2,6-diethylaniline and N-ethylaniline donors and iodine as an electron acceptor in different solvents.
2007-01
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Zoonotic cryptosporidiosis in man and animal in farms, Giza Governorate, Egypt.
2006-08
Age-related and housing-dependence of Cryptosporidium infection of calves from dairy and beef herds in South Bohemia, Czech Republic.
2006-04-30
Synthesis and reactivity of laquinimod, a quinoline-3-carboxamide: intramolecular transfer of the enol proton to a nitrogen atom as a plausible mechanism for ketene formation.
2006-02-17
Ruthenium-catalyzed intermolecular coupling reactions of arylamines with ethylene and 1,3-dienes: mechanistic insight on hydroamination vs ortho-C-H bond activation.
2005-05-26
Site of alkylation of N-methyl- and N-ethylaniline in the gas phase: a tandem mass spectrometric study.
2004-06
Selenium redox cycling in the protective effects of organoselenides against oxidant-induced DNA damage.
2004-03-03
Overtone spectra of aniline derivatives.
2004-01
Synthesis, solid-state crystal structure, and reactivity of a monomeric copper(I) anilido complex.
2003-08-06
Plausible molecular mechanism for activation by fumarate and electron transfer of the dopamine beta-mono-oxygenase reaction.
2002-10-01
Crystal structure and solid state 13C NMR analysis of N-(methyl 3,4,6-tri-O-acetyl-alpha, and beta-D-glucopyranosid-2-yl)-oxamide derivative of p-chloroaniline, N,N-diethylamine, N-methylaniline and N-ethylaniline.
2001-08-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:34:59 GMT 2025
Edited
by admin
on Mon Mar 31 19:34:59 GMT 2025
Record UNII
7E45L4I2PS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYLANILINE
MI  
Systematic Name English
N-ETHYLANILINE
HSDB  
Preferred Name English
NSC-8736
Code English
ETHYLANILINE [MI]
Common Name English
ETHYLANILINE, N-
Systematic Name English
N-ETHYLANILINE [HSDB]
Common Name English
ETHYLPHENYLAMINE
Systematic Name English
N-ETHYLBENZENAMINE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID1025271
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY
MESH
C056400
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY
CAS
103-69-5
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY
PUBCHEM
7670
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-135-5
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY
MERCK INDEX
m5089
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY Merck Index
HSDB
5354
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY
FDA UNII
7E45L4I2PS
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY
NSC
8736
Created by admin on Mon Mar 31 19:34:59 GMT 2025 , Edited by admin on Mon Mar 31 19:34:59 GMT 2025
PRIMARY