Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H21NO2S |
| Molecular Weight | 255.376 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCSC1=C(OC)C=C(CCN)C(OC)=C1
InChI
InChIKey=OLEVEPDJOFPJTF-UHFFFAOYSA-N
InChI=1S/C13H21NO2S/c1-4-7-17-13-9-11(15-2)10(5-6-14)8-12(13)16-3/h8-9H,4-7,14H2,1-3H3
| Molecular Formula | C13H21NO2S |
| Molecular Weight | 255.376 |
| 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 |
|---|---|---|
| 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 Sep |
|
| Studies on the metabolism and toxicological detection of the designer drug 4-ethyl-2,5-dimethoxy-beta-phenethylamine (2C-E) in rat urine using gas chromatographic-mass spectrometric techniques. | 2006 Oct 2 |
|
| [Analysis of the chemical drugs among structural isomer]. | 2006 Sep |
|
| Discriminative stimulus effects of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rhesus monkeys. | 2008 Feb |
|
| Discriminative stimulus effects of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rhesus monkeys: antagonism and apparent pA2 analyses. | 2009 Mar |
|
| Discriminative stimulus effects of psychostimulants and hallucinogens in S(+)-3,4-methylenedioxymethamphetamine (MDMA) and R(-)-MDMA trained mice. | 2009 Nov |
|
| Differential effects of serotonin 5-HT1A receptor agonists on the discriminative stimulus effects of the 5-HT2A receptor agonist 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rats and rhesus monkeys. | 2010 Apr |
|
| Metabolism of designer drugs of abuse: an updated review. | 2010 Jun 1 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 07:05:13 GMT 2023
by
admin
on
Sat Dec 16 07:05:13 GMT 2023
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| Record UNII |
TJG366J9BA
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| Record Status |
Validated (UNII)
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WIKIPEDIA |
Designer-drugs-2C-T-7
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DEA NO. |
7348
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WIKIPEDIA |
PiHKAL
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207740-26-9
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7554
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24728635
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DTXSID90861566
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2C-T-7
Created by
admin on Sat Dec 16 07:05:13 GMT 2023 , Edited by admin on Sat Dec 16 07:05:13 GMT 2023
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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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DB01458
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TJG366J9BA
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SALT/SOLVATE -> PARENT |
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TARGET -> AGONIST |
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ACTIVE MOIETY |
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