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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
Plausible molecular mechanism for activation by fumarate and electron transfer of the dopamine beta-mono-oxygenase reaction.
2002 Oct 1
Synthesis, solid-state crystal structure, and reactivity of a monomeric copper(I) anilido complex.
2003 Aug 6
Overtone spectra of aniline derivatives.
2004 Jan
Site of alkylation of N-methyl- and N-ethylaniline in the gas phase: a tandem mass spectrometric study.
2004 Jun
Selenium redox cycling in the protective effects of organoselenides against oxidant-induced DNA damage.
2004 Mar 3
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 Feb 17
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006 Nov
Sensory properties and color measurements of dietary chocolates with different compositions during storage for up to 360 days.
2009
(S,R,Rp)-N,N-Dimethyl-1-{2-[(1-phenyl-ethyl)amino-meth-yl]ferrocen-yl}ethanamine.
2009 Mar 25
Prevalence and molecular characterization of Cryptosporidium spp. in dairy cattle in South Bohemia, the Czech Republic.
2009 Oct 28
(R)-1-Phenyl-ethyl-ammonium trifluoro-acetate.
2010 Apr 21
4-Ethyl-anilinium perchlorate-18-crown-6 (1/1).
2010 Aug 11
In situ STM study of the adsorption and electropolymerization of o-, m-, and p-ethylaniline molecules on Au(111) electrode.
2010 Aug 28
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:11:31 GMT 2023
Edited
by admin
on Fri Dec 15 19:11:31 GMT 2023
Record UNII
7E45L4I2PS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYLANILINE
MI  
Systematic Name English
NSC-8736
Code English
ETHYLANILINE [MI]
Common Name English
ETHYLANILINE, N-
Systematic Name English
N-ETHYLANILINE
HSDB  
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 Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
MESH
C056400
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
CAS
103-69-5
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
PUBCHEM
7670
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
ECHA (EC/EINECS)
203-135-5
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
MERCK INDEX
m5089
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY Merck Index
HSDB
5354
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
FDA UNII
7E45L4I2PS
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY
NSC
8736
Created by admin on Fri Dec 15 19:11:31 GMT 2023 , Edited by admin on Fri Dec 15 19:11:31 GMT 2023
PRIMARY