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Details

Stereochemistry ACHIRAL
Molecular Formula C8H11NO.ClH
Molecular Weight 173.64
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-Ethoxyaniline hydrochloride

SMILES

Cl.CCOC1=CC=C(N)C=C1

InChI

InChIKey=JVWYCUBGJVOEIZ-UHFFFAOYSA-N
InChI=1S/C8H11NO.ClH/c1-2-10-8-5-3-7(9)4-6-8;/h3-6H,2,9H2,1H3;1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C8H11NO
Molecular Weight 137.179
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
4-Eth-oxy-anilinium bromide.
2010-11-27
Arylacetamide deacetylase is a determinant enzyme for the difference in hydrolase activities of phenacetin and acetaminophen.
2010-09
4-Eth-oxy-anilinium chloride.
2010-07-07
4-Ethoxy-anilinium hexa-fluoro-phosphate monohydrate.
2010-05-26
(E)-2-Eth-oxy-6-[(4-ethoxy-phen-yl)imino-meth-yl]phenol.
2010-02-24
(E)-2-[(4-Ethoxy-phen-yl)imino-meth-yl]-4-methoxy-phenol.
2009-10-10
2-[(4-Ethoxy-phen-yl)imino-meth-yl]-5-methoxy-phenol.
2009-10-10
Bis(4-ethoxy-anilinium) sulfate trihydrate.
2009-09-26
4-Ethoxy-anilinium perchlorate.
2009-09-05
Switchable V-type [2]pseudorotaxanes.
2009-08-06
1-[(6-Chloro-3-pyrid-yl)meth-yl]-N-(4-ethoxy-phen-yl)-3-phenyl-1H-pyrazole-5-carboxamide.
2009-03-25
Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases).
2009-03
4-Eth-oxy-N-(3-phenyl-prop-2-enyl-idene)aniline.
2008-05-17
(Z)-Methyl 3-(4-ethoxy-anilino)but-2-enoate.
2008-05-10
Mouse N-acetyltransferase type 2, the homologue of human N-acetyltransferase type 1.
2008-04-01
Immune-mediated inflammatory diseases (IMIDs) and biologic therapy: a medical revolution.
2007-04
Nanoscale amphiphilic macromolecules as lipoprotein inhibitors: the role of charge and architecture.
2007
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005-06
Effects of phenacetin and its metabolite p-phenetidine on COX-1 and COX-2 activities and expression in vitro.
2003-06-15
Inhalation toxicity of 4-ethoxyaniline (p-phenetidine): critical analysis of results of subacute inhalation exposure studies in rats.
2001-11
The role of N-hydroxyphenetidine in phenacetin-induced hemolytic anemia.
1991-10
Patents
Substance Class Chemical
Created
by admin
on Tue Apr 01 19:12:12 GMT 2025
Edited
by admin
on Tue Apr 01 19:12:12 GMT 2025
Record UNII
HB35SY9PWK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
p-Ethoxyaniline hydrochloride
Preferred Name English
4-Ethoxyaniline hydrochloride
Systematic Name English
Benzenamine, 4-ethoxy-, hydrochloride (1:1)
Systematic Name English
Benzenamine, 4-ethoxy-, hydrochloride
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
211-292-6
Created by admin on Tue Apr 01 19:12:12 GMT 2025 , Edited by admin on Tue Apr 01 19:12:12 GMT 2025
PRIMARY
EPA CompTox
DTXSID6060923
Created by admin on Tue Apr 01 19:12:12 GMT 2025 , Edited by admin on Tue Apr 01 19:12:12 GMT 2025
PRIMARY
CAS
637-56-9
Created by admin on Tue Apr 01 19:12:12 GMT 2025 , Edited by admin on Tue Apr 01 19:12:12 GMT 2025
PRIMARY
PUBCHEM
69478
Created by admin on Tue Apr 01 19:12:12 GMT 2025 , Edited by admin on Tue Apr 01 19:12:12 GMT 2025
PRIMARY
FDA UNII
HB35SY9PWK
Created by admin on Tue Apr 01 19:12:12 GMT 2025 , Edited by admin on Tue Apr 01 19:12:12 GMT 2025
PRIMARY