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(Cl)=C(Cl)C=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
Sat Dec 16 10:35:48 UTC 2023
by
admin
on
Sat Dec 16 10:35:48 UTC 2023
|
| Record UNII |
V7SQE82R87
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WIKIPEDIA |
Designer-drugs-Dichloropane
Created by
admin on Sat Dec 16 10:35:48 UTC 2023 , Edited by admin on Sat Dec 16 10:35:48 UTC 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
V7SQE82R87
Created by
admin on Sat Dec 16 10:35:48 UTC 2023 , Edited by admin on Sat Dec 16 10:35:48 UTC 2023
|
PRIMARY | |||
|
127024
Created by
admin on Sat Dec 16 10:35:48 UTC 2023 , Edited by admin on Sat Dec 16 10:35:48 UTC 2023
|
PRIMARY | |||
|
DTXSID20932894
Created by
admin on Sat Dec 16 10:35:48 UTC 2023 , Edited by admin on Sat Dec 16 10:35:48 UTC 2023
|
PRIMARY | |||
|
DICHLOROPANE
Created by
admin on Sat Dec 16 10:35:48 UTC 2023 , Edited by admin on Sat Dec 16 10:35:48 UTC 2023
|
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 Sat Dec 16 10:35:48 UTC 2023 , Edited by admin on Sat Dec 16 10:35:48 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |
