Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H13N.ClH |
| Molecular Weight | 219.71 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.NC(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=CIHWJRSPVJBHGT-UHFFFAOYSA-N
InChI=1S/C13H13N.ClH/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12;/h1-10,13H,14H2;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 | C13H13N |
| Molecular Weight | 183.249 |
| 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 |
|---|---|---|
| N-8-Substituted benztropinamine analogs as selective dopamine transporter ligands. | 2005 Dec 15 |
|
| 4-(4-Bromo-benzyl-ideneamino)-1-(diphenyl-amino-meth-yl)-3-[1-(4-isobutyl-phen-yl)eth-yl]-1H-1,2,4-triazole-5(4H)-thione. | 2008 May 7 |
|
| Palladium-catalyzed benzylic arylation of N-benzylxanthone imine. | 2008 Oct 16 |
|
| Preparation of honeycomb scaffold with hierarchical porous structures by core-crosslinked core-corona nanoparticles. | 2009 Apr 1 |
|
| Design and combinatorial synthesis of a library of methylenesulfonamides and related compounds as potential kinase inhibitors. | 2009 Mar |
|
| Benzhydrylamine linker grafting: a strategy for the improved synthesis of C-terminal peptide amides. | 2010 Oct |
|
| Synthesis and comparative properties of two amide-generating resin linkers for use in solid phase peptide synthesis. | 2010 Oct |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:52:38 GMT 2023
by
admin
on
Sat Dec 16 11:52:38 GMT 2023
|
| Record UNII |
LZ568SDT78
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
78921
Created by
admin on Sat Dec 16 11:52:38 GMT 2023 , Edited by admin on Sat Dec 16 11:52:38 GMT 2023
|
PRIMARY | |||
|
DTXSID00200644
Created by
admin on Sat Dec 16 11:52:38 GMT 2023 , Edited by admin on Sat Dec 16 11:52:38 GMT 2023
|
PRIMARY | |||
|
18792
Created by
admin on Sat Dec 16 11:52:38 GMT 2023 , Edited by admin on Sat Dec 16 11:52:38 GMT 2023
|
PRIMARY | |||
|
LZ568SDT78
Created by
admin on Sat Dec 16 11:52:38 GMT 2023 , Edited by admin on Sat Dec 16 11:52:38 GMT 2023
|
PRIMARY | |||
|
226-084-0
Created by
admin on Sat Dec 16 11:52:38 GMT 2023 , Edited by admin on Sat Dec 16 11:52:38 GMT 2023
|
PRIMARY | |||
|
5267-34-5
Created by
admin on Sat Dec 16 11:52:38 GMT 2023 , Edited by admin on Sat Dec 16 11:52:38 GMT 2023
|
PRIMARY |