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
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
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
Title | Date | PubMed |
---|---|---|
The role of N-hydroxyphenetidine in phenacetin-induced hemolytic anemia. | 1991 Oct |
|
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 |
|
Nanoscale amphiphilic macromolecules as lipoprotein inhibitors: the role of charge and architecture. | 2007 |
|
Immune-mediated inflammatory diseases (IMIDs) and biologic therapy: a medical revolution. | 2007 Apr |
|
Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases). | 2009 Mar |
|
Bis(4-ethoxy-anilinium) sulfate trihydrate. | 2009 Sep 26 |
|
4-Ethoxy-anilinium perchlorate. | 2009 Sep 5 |
|
(E)-2-Eth-oxy-6-[(4-ethoxy-phen-yl)imino-meth-yl]phenol. | 2010 Feb 24 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 12:25:55 GMT 2023
by
admin
on
Sat Dec 16 12:25:55 GMT 2023
|
Record UNII |
HB35SY9PWK
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
211-292-6
Created by
admin on Sat Dec 16 12:25:55 GMT 2023 , Edited by admin on Sat Dec 16 12:25:55 GMT 2023
|
PRIMARY | |||
|
DTXSID6060923
Created by
admin on Sat Dec 16 12:25:55 GMT 2023 , Edited by admin on Sat Dec 16 12:25:55 GMT 2023
|
PRIMARY | |||
|
637-56-9
Created by
admin on Sat Dec 16 12:25:55 GMT 2023 , Edited by admin on Sat Dec 16 12:25:55 GMT 2023
|
PRIMARY | |||
|
69478
Created by
admin on Sat Dec 16 12:25:55 GMT 2023 , Edited by admin on Sat Dec 16 12:25:55 GMT 2023
|
PRIMARY | |||
|
HB35SY9PWK
Created by
admin on Sat Dec 16 12:25:55 GMT 2023 , Edited by admin on Sat Dec 16 12:25:55 GMT 2023
|
PRIMARY |