Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C11H15NO2.ClH |
| Molecular Weight | 229.703 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCOC(=O)C(N)CC1=CC=CC=C1
InChI
InChIKey=FPFQPLFYTKMCHN-UHFFFAOYSA-N
InChI=1S/C11H15NO2.ClH/c1-2-14-11(13)10(12)8-9-6-4-3-5-7-9;/h3-7,10H,2,8,12H2,1H3;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 | C11H15NO2 |
| Molecular Weight | 193.2423 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 18:06:53 GMT 2025
by
admin
on
Wed Apr 02 18:06:53 GMT 2025
|
| Record UNII |
8M4M6Q8LLU
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID10941733
Created by
admin on Wed Apr 02 18:06:53 GMT 2025 , Edited by admin on Wed Apr 02 18:06:53 GMT 2025
|
PRIMARY | |||
|
8M4M6Q8LLU
Created by
admin on Wed Apr 02 18:06:53 GMT 2025 , Edited by admin on Wed Apr 02 18:06:53 GMT 2025
|
PRIMARY | |||
|
19881-53-9
Created by
admin on Wed Apr 02 18:06:53 GMT 2025 , Edited by admin on Wed Apr 02 18:06:53 GMT 2025
|
PRIMARY | |||
|
11333686
Created by
admin on Wed Apr 02 18:06:53 GMT 2025 , Edited by admin on Wed Apr 02 18:06:53 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ENANTIOMER -> RACEMATE |
|
||
|
ENANTIOMER -> RACEMATE |
|