Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C9H12ClN |
| Molecular Weight | 169.651 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(N)CC1=CC=C(Cl)C=C1
InChI
InChIKey=WWPITPSIWMXDPE-UHFFFAOYSA-N
InChI=1S/C9H12ClN/c1-7(11)6-8-2-4-9(10)5-3-8/h2-5,7H,6,11H2,1H3
| Molecular Formula | C9H12ClN |
| Molecular Weight | 169.651 |
| 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
Mon Mar 31 22:52:47 GMT 2025
by
admin
on
Mon Mar 31 22:52:47 GMT 2025
|
| Record UNII |
897NVD4A52
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WIKIPEDIA |
Designer-drugs-4-CA
Created by
admin on Mon Mar 31 22:52:47 GMT 2025 , Edited by admin on Mon Mar 31 22:52:47 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
PARA-CHLOROAMPHETAMINE
Created by
admin on Mon Mar 31 22:52:47 GMT 2025 , Edited by admin on Mon Mar 31 22:52:47 GMT 2025
|
PRIMARY | para-Chloroamphetamine (PCA), also known as 4-chloroamphetamine (4-CA), is an amphetamine derivative and monoamine releaser similar to MDMA, but with substantially higher neurotoxicity, thought to be due to the unrestrained release of both serotonin and dopamine by a metabolite. It is used as a neurotoxin by neurobiologists to selectively kill serotonergic neurons for research purposes, in the same way that 6-hydroxydopamine is used to kill dopaminergic neurons. However, the effects of the compound on experimental animals appear less encouraging.[6] It has been detected as an apparent designer drug, along with the related 3-chloroamphetamine, which is even more potent as a releaser of dopamine and serotonin but slightly less neurotoxic. | ||
|
897NVD4A52
Created by
admin on Mon Mar 31 22:52:47 GMT 2025 , Edited by admin on Mon Mar 31 22:52:47 GMT 2025
|
PRIMARY | |||
|
3127
Created by
admin on Mon Mar 31 22:52:47 GMT 2025 , Edited by admin on Mon Mar 31 22:52:47 GMT 2025
|
PRIMARY | |||
|
287208
Created by
admin on Mon Mar 31 22:52:47 GMT 2025 , Edited by admin on Mon Mar 31 22:52:47 GMT 2025
|
PRIMARY | |||
|
DTXSID90897229
Created by
admin on Mon Mar 31 22:52:47 GMT 2025 , Edited by admin on Mon Mar 31 22:52:47 GMT 2025
|
PRIMARY | |||
|
64-12-0
Created by
admin on Mon Mar 31 22:52:47 GMT 2025 , Edited by admin on Mon Mar 31 22:52:47 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ENANTIOMER -> RACEMATE |
|
||
|
ENANTIOMER -> RACEMATE |
|
||
|
SALT/SOLVATE -> PARENT |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |
|