Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C17H17NO3.ClH |
| Molecular Weight | 319.783 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(NCC1=CC=CC=C1)C(=O)C2=CC=C3OCOC3=C2
InChI
InChIKey=VPHHNGQFGIQHOU-UHFFFAOYSA-N
InChI=1S/C17H17NO3.ClH/c1-12(18-10-13-5-3-2-4-6-13)17(19)14-7-8-15-16(9-14)21-11-20-15;/h2-9,12,18H,10-11H2,1H3;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 | C17H17NO3 |
| Molecular Weight | 283.3218 |
| 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 13:15:05 GMT 2025
by
admin
on
Wed Apr 02 13:15:05 GMT 2025
|
| Record UNII |
LC23C39YAY
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
LC23C39YAY
Created by
admin on Wed Apr 02 13:15:05 GMT 2025 , Edited by admin on Wed Apr 02 13:15:05 GMT 2025
|
PRIMARY | |||
|
1823274-68-5
Created by
admin on Wed Apr 02 13:15:05 GMT 2025 , Edited by admin on Wed Apr 02 13:15:05 GMT 2025
|
PRIMARY | |||
|
DTXSID701341945
Created by
admin on Wed Apr 02 13:15:05 GMT 2025 , Edited by admin on Wed Apr 02 13:15:05 GMT 2025
|
PRIMARY | |||
|
Benzylone
Created by
admin on Wed Apr 02 13:15:05 GMT 2025 , Edited by admin on Wed Apr 02 13:15:05 GMT 2025
|
PRIMARY | |||
|
129318251
Created by
admin on Wed Apr 02 13:15:05 GMT 2025 , Edited by admin on Wed Apr 02 13:15:05 GMT 2025
|
PRIMARY |