Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C14H17NS2.ClH |
| Molecular Weight | 299.882 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CC(C=C(C1=CC=CS1)C2=CC=CS2)N(C)C
InChI
InChIKey=OBFGNODOJKVYIR-UHFFFAOYSA-N
InChI=1S/C14H17NS2.ClH/c1-11(15(2)3)10-12(13-6-4-8-16-13)14-7-5-9-17-14;/h4-11H,1-3H3;1H
| Molecular Formula | C14H17NS2 |
| Molecular Weight | 263.421 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
| 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 |
Dimethylthiambutene is the synthetic narcotic analgesic agent. It has analgesic effect similar to those of meperidine. The (+)-enantiomer of dimethylthiambutene is more active than the (-)-isomer. Dimethylthiambutene clinically compared with meperidine (pethidine), but maintains the dependence-producing capability of morphine. It has had illicit use in Japan in the past. Dimethylthiambutene is under international control according to the UN Single Convention 1961 and its amendments, Schedule I.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:56:08 UTC 2023
by
admin
on
Sat Dec 16 10:56:08 UTC 2023
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| Record UNII |
ZI2995I73Y
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| Record Status |
Validated (UNII)
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| Record Version |
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ZI2995I73Y
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22028
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5786-77-6
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m1119
Created by
admin on Sat Dec 16 10:56:08 UTC 2023 , Edited by admin on Sat Dec 16 10:56:08 UTC 2023
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DTXSID20973449
Created by
admin on Sat Dec 16 10:56:08 UTC 2023 , Edited by admin on Sat Dec 16 10:56:08 UTC 2023
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ACTIVE MOIETY |