Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H11N |
Molecular Weight | 181.2331 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C(=N\C1=CC=CC=C1)\C2=CC=CC=C2
InChI
InChIKey=UVEWQKMPXAHFST-KAMYIIQDSA-N
InChI=1S/C13H11N/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13/h1-11H/b14-11-
Molecular Formula | C13H11N |
Molecular Weight | 181.2331 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Synthesis of polycyclic structures by the Diels-Alder reaction of inner-outer-ring 1,3-bis(trimethylsilyloxy)dienes. | 2001 Feb 23 |
|
Torsional vibration and central bond length of N-benzylideneanilines. | 2004 Oct |
|
Theoretical studies on the role of pi-electron delocalization in determining the conformation of N-benzylideneaniline with three types of LMO basis sets. | 2006 May |
|
Mechanistic investigations of imine hydrogenation catalyzed by dinuclear iridium complexes. | 2006 May 15 |
|
Aza-stilbenes as potent and selective c-RAF inhibitors. | 2006 Oct 15 |
|
Insight into the free-radical-scavenging mechanism of hydroxyl-substituent Schiff bases in the free-radical-induced hemolysis of erythrocytes. | 2007 Nov-Dec |
|
Antiproliferative effects of some N-benzylideneanilines. | 2008 Jan-Feb |
|
Cycloreversion of azetidines via oxidative electron transfer. steady-state and time-resolved studies. | 2008 Nov 20 |
|
(E)-4-[(4-Methoxy-phen-yl)imino-meth-yl]-N,N-dimethyl-aniline. | 2009 Feb 6 |
|
Fluorescent chemosensors for toxic organophosphorus pesticides: a review. | 2010 |
|
DFT study of linear and nonlinear optical properties of donor-acceptor substituted stilbenes, azobenzenes and benzilideneanilines. | 2010 Apr |
|
Adsorption and switching properties of a N-benzylideneaniline based molecular switch on a Au(111) surface. | 2010 Jul 28 |
|
Eco-contribution for the production of N-arylnitrones: solvent-free and assisted by microwaves. | 2010 Jun 22 |
|
Heterolytic H2 activation by rhodium thiolato complexes bearing the hydrotris(pyrazolyl)borato ligand and application to catalytic hydrogenation under mild conditions. | 2010 Mar 28 |
|
Two isomorphous azastilbene derivatives: 1-(2-chlorobenzyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]pyridinium chloride and 1-(2-bromobenzyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]pyridinium bromide. | 2010 Oct |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:00:44 GMT 2023
by
admin
on
Sat Dec 16 10:00:44 GMT 2023
|
Record UNII |
M1JG410QVC
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
M1JG410QVC
Created by
admin on Sat Dec 16 10:00:44 GMT 2023 , Edited by admin on Sat Dec 16 10:00:44 GMT 2023
|
PRIMARY | |||
|
DTXSID30871760
Created by
admin on Sat Dec 16 10:00:44 GMT 2023 , Edited by admin on Sat Dec 16 10:00:44 GMT 2023
|
PRIMARY | |||
|
33993-35-0
Created by
admin on Sat Dec 16 10:00:44 GMT 2023 , Edited by admin on Sat Dec 16 10:00:44 GMT 2023
|
PRIMARY | |||
|
m2411
Created by
admin on Sat Dec 16 10:00:44 GMT 2023 , Edited by admin on Sat Dec 16 10:00:44 GMT 2023
|
PRIMARY |