Details
| Stereochemistry | UNKNOWN |
| Molecular Formula | C11H12Cl3N |
| Molecular Weight | 264.579 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(CC1=CC=CC=C1)\N=C\C(Cl)(Cl)Cl
InChI
InChIKey=VBZDETYCYXPOAK-OVCLIPMQSA-N
InChI=1S/C11H12Cl3N/c1-9(15-8-11(12,13)14)7-10-5-3-2-4-6-10/h2-6,8-9H,7H2,1H3/b15-8+
| Molecular Formula | C11H12Cl3N |
| Molecular Weight | 264.579 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Optical Activity | ( + / - ) |
Amphecloral (INN: amfecloral) is a phenethylamine derivative which was patented in 1960 as an amphetamine pro-drug with prolonged duration of action. Amfecloral was used as an appetite suppressant under the trade name Acutran, but is now no longer marketed. It is an anorectic drug with little to no stimulant activity. Amphecloral is metabolized to both d-(S)- and l-(R)-amphetamine.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 18:47:28 GMT 2023
by
admin
on
Sat Dec 16 18:47:28 GMT 2023
|
| Record UNII |
S0DYI19OEX
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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S0DYI19OEX
Created by
admin on Sat Dec 16 18:47:28 GMT 2023 , Edited by admin on Sat Dec 16 18:47:28 GMT 2023
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71528-69-3
Created by
admin on Sat Dec 16 18:47:28 GMT 2023 , Edited by admin on Sat Dec 16 18:47:28 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
