Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H19NO2 |
| Molecular Weight | 209.2848 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=CC(OC)=C(CCN)C=C1OC
InChI
InChIKey=VDRGNAMREYBIHA-UHFFFAOYSA-N
InChI=1S/C12H19NO2/c1-4-9-7-12(15-3)10(5-6-13)8-11(9)14-2/h7-8H,4-6,13H2,1-3H3
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 |
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| The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. | 2007-03-22 |
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| 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 |
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Preferred Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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WIKIPEDIA |
PiHKAL
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admin on Mon Mar 31 23:03:49 GMT 2025 , Edited by admin on Mon Mar 31 23:03:49 GMT 2025
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WIKIPEDIA |
Designer-drugs-2C-E
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admin on Mon Mar 31 23:03:49 GMT 2025 , Edited by admin on Mon Mar 31 23:03:49 GMT 2025
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DEA NO. |
7509
Created by
admin on Mon Mar 31 23:03:49 GMT 2025 , Edited by admin on Mon Mar 31 23:03:49 GMT 2025
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| Code System | Code | Type | Description | ||
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I190284UXX
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PRIMARY | |||
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DTXSID40221772
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PRIMARY | |||
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71539-34-9
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admin on Mon Mar 31 23:03:49 GMT 2025 , Edited by admin on Mon Mar 31 23:03:49 GMT 2025
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PRIMARY | |||
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2C-E
Created by
admin on Mon Mar 31 23:03:49 GMT 2025 , Edited by admin on Mon Mar 31 23:03:49 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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24729233
Created by
admin on Mon Mar 31 23:03:49 GMT 2025 , Edited by admin on Mon Mar 31 23:03:49 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)
