Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H11N.ClH |
| Molecular Weight | 217.694 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.N=C(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=QXHZCMMSAPYFKT-UHFFFAOYSA-N
InChI=1S/C13H11N.ClH/c14-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12;/h1-10,14H;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 | C13H11N |
| Molecular Weight | 181.2331 |
| 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 |
|---|---|---|
| An efficient catalyst system for Pd-catalyzed amination of [2.2]paracyclophanyl bromides. | 2009-09-04 |
|
| Azido-(1,1-diphenyl-methanimine-κN)[hydridotris(pyrazolyl-κN)borato](triphenyl-phosphine-κP)ruthenium(II) diethyl ether solvate. | 2008-11-08 |
|
| First example of the solid-state thermal cyclometalation of ligated benzophenone imine giving novel luminescent platinum(II) species. | 2007-05-28 |
|
| Redox-induced terpyridyl substitution in the Os(VI)-hydrazido complex, trans-[Os(VI)(tpy)(Cl)(2)(NN(CH(2))(4)O)](2+). | 2001-07-30 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:06:59 GMT 2025
by
admin
on
Mon Mar 31 22:06:59 GMT 2025
|
| Record UNII |
M8RM3S474H
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
143525
Created by
admin on Mon Mar 31 22:06:59 GMT 2025 , Edited by admin on Mon Mar 31 22:06:59 GMT 2025
|
PRIMARY | |||
|
M8RM3S474H
Created by
admin on Mon Mar 31 22:06:59 GMT 2025 , Edited by admin on Mon Mar 31 22:06:59 GMT 2025
|
PRIMARY | |||
|
m2372
Created by
admin on Mon Mar 31 22:06:59 GMT 2025 , Edited by admin on Mon Mar 31 22:06:59 GMT 2025
|
PRIMARY | Merck Index | ||
|
12234619
Created by
admin on Mon Mar 31 22:06:59 GMT 2025 , Edited by admin on Mon Mar 31 22:06:59 GMT 2025
|
PRIMARY | |||
|
5319-67-5
Created by
admin on Mon Mar 31 22:06:59 GMT 2025 , Edited by admin on Mon Mar 31 22:06:59 GMT 2025
|
PRIMARY | |||
|
DTXSID10201248
Created by
admin on Mon Mar 31 22:06:59 GMT 2025 , Edited by admin on Mon Mar 31 22:06:59 GMT 2025
|
PRIMARY |