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
Mon Mar 31 23:30:58 GMT 2025
by
admin
on
Mon Mar 31 23:30:58 GMT 2025
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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
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admin on Mon Mar 31 23:30:58 GMT 2025 , Edited by admin on Mon Mar 31 23:30:58 GMT 2025
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DTXSID20973449
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admin on Mon Mar 31 23:30:58 GMT 2025 , Edited by admin on Mon Mar 31 23:30:58 GMT 2025
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PARENT -> SALT/SOLVATE |
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ACTIVE MOIETY |