Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H19NO2S |
| Molecular Weight | 241.35 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCSC1=CC(OC)=C(CCN)C=C1OC
InChI
InChIKey=HCWQGDLBIKOJPM-UHFFFAOYSA-N
InChI=1S/C12H19NO2S/c1-4-16-12-8-10(14-2)9(5-6-13)7-11(12)15-3/h7-8H,4-6,13H2,1-3H3
| Molecular Formula | C12H19NO2S |
| Molecular Weight | 241.35 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Metabolism of designer drugs of abuse: an updated review. | 2010-06-01 |
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| Liquid chromatography-atmospheric pressure ionization electrospray mass spectrometry determination of "hallucinogenic designer drugs" in urine of consumers. | 2008-06-09 |
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| Determination of four thiophenethylamine designer drugs (2C-T-series) in human plasma by capillary electrophoresis with mass spectrometry detection. | 2007-08-03 |
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| Optimization of the separation and on-line sample concentration of phenethylamine designer drugs with capillary electrophoresis-fluorescence detection. | 2006-01-06 |
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| New designer drug 2,5-dimethoxy-4-ethylthio-beta-phenethylamine (2C-T-2): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry. | 2005-09 |
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| The bioactivity of 2,5-dimethoxy-4-ethylthiophenethylamine (2C-T-2) and its detection in rat urine by capillary electrophoresis combined with an on-line sample concentration technique. | 2004-11-25 |
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| Identification of 2,5-dimethoxy-4-ethylthiophenethylamine and its metabolites in the urine of rats by gas chromatography-mass spectrometry. | 2003-12-25 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Tue Apr 01 16:21:24 GMT 2025
by
admin
on
Tue Apr 01 16:21:24 GMT 2025
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| Record UNII |
WPS2KSX2TJ
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| Record Status |
Validated (UNII)
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WIKIPEDIA |
Designer-drugs-2C-T-2
Created by
admin on Tue Apr 01 16:21:24 GMT 2025 , Edited by admin on Tue Apr 01 16:21:24 GMT 2025
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WIKIPEDIA |
PiHKAL
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admin on Tue Apr 01 16:21:24 GMT 2025 , Edited by admin on Tue Apr 01 16:21:24 GMT 2025
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DEA NO. |
7385
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| Code System | Code | Type | Description | ||
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207740-24-7
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PRIMARY | |||
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WPS2KSX2TJ
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PRIMARY | |||
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DTXSID40174850
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admin on Tue Apr 01 16:21:24 GMT 2025 , Edited by admin on Tue Apr 01 16:21:24 GMT 2025
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PRIMARY | |||
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2C-T-2
Created by
admin on Tue Apr 01 16:21:24 GMT 2025 , Edited by admin on Tue Apr 01 16:21:24 GMT 2025
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PRIMARY | 2C (2C-x) is a general name for the family of psychedelic phenethylamines containing methoxy groups on the 2 and 5 positions of a benzene ring. Most of these compounds also carry lipophilic substituents at the 4 position, usually resulting in more potent and more metabolically stable and longer acting compounds. Most of the currently known 2C compounds were first synthesized by Alexander Shulgin in the 1970s and 1980s, and published in his book, PiHKAL (Phenethylamines i Have Known And Loved). Dr. Shulgin also invented the term 2C, being an acronym for the 2 carbon atoms between the benzene ring and the amino group.[1] Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. | ||
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12074193
Created by
admin on Tue Apr 01 16:21:24 GMT 2025 , Edited by admin on Tue Apr 01 16:21:24 GMT 2025
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |
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