Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H16N2 |
| Molecular Weight | 212.2902 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C(CNC1=CC=CC=C1)NC2=CC=CC=C2
InChI
InChIKey=NOUUUQMKVOUUNR-UHFFFAOYSA-N
InChI=1S/C14H16N2/c1-3-7-13(8-4-1)15-11-12-16-14-9-5-2-6-10-14/h1-10,15-16H,11-12H2
| Molecular Formula | C14H16N2 |
| Molecular Weight | 212.2902 |
| 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 |
|---|---|---|
| Enantioselective Michael addition of ketones to maleimides catalyzed by bifunctional monosulfonyl DPEN salt. | 2010-07-07 |
|
| Preparation and enantioseparation of a mixed selector chiral stationary phase derived from benzoylated tartaric acid and 1,2-diphenylethylenediamine. | 2010-06 |
|
| Selective formation of cis-diacyl, cis-PPh(2)R rhodium(III) complexes by the reaction of rhodium(III) cis-diacyl, trans-PPh(2)R complexes with aliphatic diamines. | 2009-11-28 |
|
| Synthesis and characterization of some chiral metal-salen complexes bearing a ferrocenophane substituent. | 2009-10-26 |
|
| Synthesis of dendritic stationary phases with surface-bonded L-phenylalanine derivate as chiral selector and their evaluation in HPLC resolution of racemic compounds. | 2008-07 |
|
| Tuning mechanism in a two-component columnar host system composed of 1,2-diphenylethylenediamine and 1,1'-binaphthyl-2,2'-dicarboxylic acid. | 2008-02-07 |
|
| Synthesis of polymer-type chiral stationary phases and their enantioseparation evaluation by high-performance liquid chromatography. | 2007-02 |
|
| Preparation of polymer-supported Ru-TsDPEN catalysts and use for enantioselective synthesis of (S)-fluoxetine. | 2005-07-21 |
|
| Determination of serotonin, noradrenaline, dopamine and their metabolites in rat brain extracts and microdialysis samples by column liquid chromatography with fluorescence detection following derivatization with benzylamine and 1,2-diphenylethylenediamine. | 2004-08-05 |
|
| Simultaneous determination of 5-hydroxyindoles and catechols by high-performance liquid chromatography with fluorescence detection following derivatization with benzylamine and 1,2-diphenylethylenediamine. | 2003-09-19 |
|
| Spectrofluorometric determination of catechins with 1,2-diphenylethylenediamine. | 2002-08 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:56:27 GMT 2025
by
admin
on
Mon Mar 31 18:56:27 GMT 2025
|
| Record UNII |
PXK7AM35L2
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
205-765-6
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY | |||
|
C007305
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY | |||
|
DTXSID1059739
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY | |||
|
m4260
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY | Merck Index | ||
|
8719
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY | |||
|
150-61-8
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY | |||
|
PXK7AM35L2
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY | |||
|
67422
Created by
admin on Mon Mar 31 18:56:27 GMT 2025 , Edited by admin on Mon Mar 31 18:56:27 GMT 2025
|
PRIMARY |