Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H21NO2S.ClH |
| Molecular Weight | 291.837 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCCSC1=CC(OC)=C(CCN)C=C1OC
InChI
InChIKey=AHZKNSBEESCMGM-UHFFFAOYSA-N
InChI=1S/C13H21NO2S.ClH/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;1H
| 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 |
| 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 |
|---|---|---|
| Metabolism of designer drugs of abuse: an updated review. | 2010-06-01 |
|
| 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. | 2010-04 |
|
| Discriminative stimulus effects of psychostimulants and hallucinogens in S(+)-3,4-methylenedioxymethamphetamine (MDMA) and R(-)-MDMA trained mice. | 2009-11 |
|
| Discriminative stimulus effects of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rhesus monkeys: antagonism and apparent pA2 analyses. | 2009-03 |
|
| Discriminative stimulus effects of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rhesus monkeys. | 2008-02 |
|
| Determination of four thiophenethylamine designer drugs (2C-T-series) in human plasma by capillary electrophoresis with mass spectrometry detection. | 2007-08-03 |
|
| In vivo metabolism of 2,5-dimethoxy-4-propylthiophenethylamine in rat. | 2007-06 |
|
| 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. | 2006-10-02 |
|
| [Analysis of the chemical drugs among structural isomer]. | 2006-09 |
|
| Optimization of the separation and on-line sample concentration of phenethylamine designer drugs with capillary electrophoresis-fluorescence detection. | 2006-01-06 |
|
| New trends in the cyber and street market of recreational drugs? The case of 2C-T-7 ('Blue Mystic'). | 2005-11 |
|
| 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 |
|
| Hallucinogen-like actions of 2,5-dimethoxy-4-(n)-propylthiophenethylamine (2C-T-7) in mice and rats. | 2005-09 |
|
| New designer drug, 2,5-dimethoxy-4-propylthio-beta-phenethylamine (2C-T-7): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry. | 2005-01 |
|
| Schedules of controlled substances; placement of 2,5-dimethoxy-4-(n)-propylthiophenethylamine and N-benzylpiperazine into Schedule I of the Controlled Substances Act. Final rule. | 2004-03-18 |
|
| Postmortem identification and quantitation of 2,5-dimethoxy-4-n-propylthiophenethylamine using GC-MSD and GC-NPD. | 2003-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:00:13 GMT 2025
by
admin
on
Mon Mar 31 22:00:13 GMT 2025
|
| Record UNII |
70O70T990D
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
DTXSID2048878
Created by
admin on Mon Mar 31 22:00:13 GMT 2025 , Edited by admin on Mon Mar 31 22:00:13 GMT 2025
|
PRIMARY | |||
|
46781343
Created by
admin on Mon Mar 31 22:00:13 GMT 2025 , Edited by admin on Mon Mar 31 22:00:13 GMT 2025
|
PRIMARY | |||
|
850140-15-7
Created by
admin on Mon Mar 31 22:00:13 GMT 2025 , Edited by admin on Mon Mar 31 22:00:13 GMT 2025
|
PRIMARY | |||
|
70O70T990D
Created by
admin on Mon Mar 31 22:00:13 GMT 2025 , Edited by admin on Mon Mar 31 22:00:13 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
ACTIVE MOIETY |
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.
|