Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H11N |
| Molecular Weight | 133.1903 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CCC2=NC=CC=C2C1
InChI
InChIKey=YQDGQEKUTLYWJU-UHFFFAOYSA-N
InChI=1S/C9H11N/c1-2-6-9-8(4-1)5-3-7-10-9/h3,5,7H,1-2,4,6H2
| Molecular Formula | C9H11N |
| Molecular Weight | 133.1903 |
| 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 |
|---|---|---|
| 5,8-Dimeth-oxy-2-phenyl-1,4-dihydro-quinoline-3-carbonitrile. | 2010-08-18 |
|
| 8-(4-Chloro-benzyl-idene)-4-(4-chloro-phen-yl)-2-phenyl-5,6,7,8-tetra-hydro-quinoline. | 2010-05-22 |
|
| 5,6,7,8-Tetra-hydro-quinoline 1-oxide hemihydrate. | 2010-03-13 |
|
| Synthesis and characterization of 5,6,7,8-tetrahydroquinoline C5a receptor antagonists. | 2008-04-15 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:49:44 GMT 2025
by
admin
on
Mon Mar 31 19:49:44 GMT 2025
|
| Record UNII |
L786AAG56H
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
241127
Created by
admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
|
PRIMARY | |||
|
10500-57-9
Created by
admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
|
PRIMARY | |||
|
L786AAG56H
Created by
admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
|
PRIMARY | |||
|
66335
Created by
admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
|
PRIMARY | |||
|
DTXSID40146911
Created by
admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
|
PRIMARY | |||
|
234-030-2
Created by
admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
|
PRIMARY |