Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H11NO |
| Molecular Weight | 137.179 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC1=CC=C(N)C=C1
InChI
InChIKey=IMPPGHMHELILKG-UHFFFAOYSA-N
InChI=1S/C8H11NO/c1-2-10-8-5-3-7(9)4-6-8/h3-6H,2,9H2,1H3
| 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
| Title | Date | PubMed |
|---|---|---|
| The role of N-hydroxyphenetidine in phenacetin-induced hemolytic anemia. | 1991 Oct |
|
| Inhalation toxicity of 4-ethoxyaniline (p-phenetidine): critical analysis of results of subacute inhalation exposure studies in rats. | 2001 Nov |
|
| Effects of phenacetin and its metabolite p-phenetidine on COX-1 and COX-2 activities and expression in vitro. | 2003 Jun 15 |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
|
| Mouse N-acetyltransferase type 2, the homologue of human N-acetyltransferase type 1. | 2008 Apr 1 |
|
| (Z)-Methyl 3-(4-ethoxy-anilino)but-2-enoate. | 2008 May 10 |
|
| 4-Eth-oxy-N-(3-phenyl-prop-2-enyl-idene)aniline. | 2008 May 17 |
|
| Switchable V-type [2]pseudorotaxanes. | 2009 Aug 6 |
|
| Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases). | 2009 Mar |
|
| 1-[(6-Chloro-3-pyrid-yl)meth-yl]-N-(4-ethoxy-phen-yl)-3-phenyl-1H-pyrazole-5-carboxamide. | 2009 Mar 25 |
|
| 2-[(4-Ethoxy-phen-yl)imino-meth-yl]-5-methoxy-phenol. | 2009 Oct 10 |
|
| (E)-2-Eth-oxy-6-[(4-ethoxy-phen-yl)imino-meth-yl]phenol. | 2010 Feb 24 |
|
| 4-Eth-oxy-anilinium chloride. | 2010 Jul 7 |
|
| 4-Eth-oxy-anilinium bromide. | 2010 Nov 27 |
|
| Arylacetamide deacetylase is a determinant enzyme for the difference in hydrolase activities of phenacetin and acetaminophen. | 2010 Sep |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:33:02 UTC 2023
by
admin
on
Fri Dec 15 18:33:02 UTC 2023
|
| Record UNII |
9TSL224ZSE
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
3116
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | |||
|
m8612
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | Merck Index | ||
|
p-Phenetidine
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | |||
|
156-43-4
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | |||
|
85505
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | |||
|
205-855-5
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | |||
|
9TSL224ZSE
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | |||
|
9076
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY | |||
|
DTXSID0025864
Created by
admin on Fri Dec 15 18:33:02 UTC 2023 , Edited by admin on Fri Dec 15 18:33:02 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> METABOLITE TOXIC |
Metabolite induced methaemoglobinaemia in man.
|
