Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H17Cl2NO2 |
| Molecular Weight | 314.207 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)[C@@H]1[C@H]2CC[C@@H](C[C@@H]1C3=CC=C(Cl)C(Cl)=C3)N2
InChI
InChIKey=JFUNLJPTPCQLIR-PJQZNRQZSA-N
InChI=1S/C15H17Cl2NO2/c1-20-15(19)14-10(7-9-3-5-13(14)18-9)8-2-4-11(16)12(17)6-8/h2,4,6,9-10,13-14,18H,3,5,7H2,1H3/t9-,10+,13+,14-/m0/s1
| Molecular Formula | C15H17Cl2NO2 |
| Molecular Weight | 314.207 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:19:57 GMT 2025
by
admin
on
Mon Mar 31 23:19:57 GMT 2025
|
| Record UNII |
V7SQE82R87
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WIKIPEDIA |
Designer-drugs-Dichloropane
Created by
admin on Mon Mar 31 23:19:57 GMT 2025 , Edited by admin on Mon Mar 31 23:19:57 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
V7SQE82R87
Created by
admin on Mon Mar 31 23:19:57 GMT 2025 , Edited by admin on Mon Mar 31 23:19:57 GMT 2025
|
PRIMARY | |||
|
127024
Created by
admin on Mon Mar 31 23:19:57 GMT 2025 , Edited by admin on Mon Mar 31 23:19:57 GMT 2025
|
PRIMARY | |||
|
DTXSID20932894
Created by
admin on Mon Mar 31 23:19:57 GMT 2025 , Edited by admin on Mon Mar 31 23:19:57 GMT 2025
|
PRIMARY | |||
|
DICHLOROPANE
Created by
admin on Mon Mar 31 23:19:57 GMT 2025 , Edited by admin on Mon Mar 31 23:19:57 GMT 2025
|
PRIMARY | Dichloropane ((-)-2.beta.-Carbomethoxy-3.beta.-(3,4-dichlorophenyl)tropane, RTI-4229-111, O-401) is a powerful SNDRI with IC50 (nM) values of 0.79, 3.13, and 18 at the DAT, SERT, and NET. Methylecgonidine as the direct precursor to this compound. In contrast to the closely related RTI-112, dichloropane is a potent stimulant drug which produces similar effects to cocaine as well as being structurally similar to cocaine. In animal studies although, dichloropane had a slower onset and longer duration of action. | ||
|
146725-34-0
Created by
admin on Mon Mar 31 23:19:57 GMT 2025 , Edited by admin on Mon Mar 31 23:19:57 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |
