Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H19NO2.ClH |
| Molecular Weight | 245.746 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC1=C(OC)C=C(CCN)C(OC)=C1
InChI
InChIKey=CTDRFXSMYFXGIH-UHFFFAOYSA-N
InChI=1S/C12H19NO2.ClH/c1-4-9-7-12(15-3)10(5-6-13)8-11(9)14-2;/h7-8H,4-6,13H2,1-3H3;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 | C12H19NO2 |
| Molecular Weight | 209.2848 |
| 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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| In vitro screening of psychoactive drugs by [(35)S]GTPgammaS binding in rat brain membranes. | 2007-12 |
|
| The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. | 2007-03-22 |
|
| 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 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:52:55 GMT 2025
by
admin
on
Mon Mar 31 22:52:55 GMT 2025
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| Record UNII |
7OSN5S910H
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| Record Status |
Validated (UNII)
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| Record Version |
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53299307
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7OSN5S910H
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DTXSID60693270
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923013-67-6
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admin on Mon Mar 31 22:52:55 GMT 2025 , Edited by admin on Mon Mar 31 22:52:55 GMT 2025
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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.
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