| 释义 |
- Legality Canada
- See also
- References
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.[1] 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.[2] 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). Shulgin also coined the term 2C, being an acronym for the 2 carbon atoms between the benzene ring and the amino group.[3]| Nomenclature | R3 | R4 | 2D Structure | 3D Structure |
|---|
| 2C-B | H | Br | | 2C-BAN | | 2C-Bn | H | CH2C6H5 | | 2C-Bu | H | CH2CH2CH2CH3 | | 2C-C | H | Cl | | 2C-CN | H | C≡N | | 2C-CP | H | C3H5 | | 2C-D | H | CH3 | | 2C-E | H | CH2CH3 | | 2C-EF | H | CH2CH2F | | 2C-F | H | F | | 2C-G | CH3 | CH3 | | 2C-G-1 | CH2 | | 2C-G-2 | (CH2)2 | | 2C-G-3 | (CH2)3 | | 2C-G-4 | (CH2)4 | | 2C-G-5 | (CH2)5 | | 2C-G-6 | (CH2)6 | | 2C-G-N | (CH)4 | | 2C-H | H | H | | 2C-I | H | I | | 2C-iP | H | CH(CH3)2 | | 2C-N | H | NO2 | | 2C-NH2 | H | NH2 | | 2C-O | H | OCH3 | | 2C-O-4 | H | OCH(CH3)2 | | 2C-P | H | CH2CH2CH3 | | 2C-Ph | H | C6H5 | | 2C-SE | H | Se CH3 | | 2C-T | H | SCH3 | | 2C-T-2 | H | SCH2CH3 | | 2C-T-3[4] | | 2C-T-4 | H | SCH(CH3)2 | | 2C-T-5[4] | | 2C-T-6[4] | | 2C-T-7 | H | S(CH2)2CH3 | | 2C-T-8 | H | SCH2CH(CH2)2 | | 2C-T-9[4] | | 2C-T-10[4] | | 2C-T-11[4] | | 2C-T-12[4] | | 2C-T-13 | H | S(CH2)2OCH3 | | 2C-T-14[5] | | 2C-T-15 | H | SCH(CH2)2 | | 2C-T-16 | H | SCH2CH=CH2 | | 2C-T-17 | H | SCH(CH3)CH2CH3 | | 2C-T-18[5] | | 2C-T-19 | H | SCH2CH2CH2CH3 | | 2C-T-20[5] | | 2C-T-21 | H | S(CH2)2F | | 2C-T-21.5[5] | | 2C-T-22[5] | | 2C-T-23[5] | | 2C-T-24[5] | | 2C-T-25[5] | | 2C-T-27[5] | | 2C-T-28[5] | | 2C-T-30[5] | | 2C-T-31[5] | | 2C-T-32[5] | | 2C-T-33[5] | | 2C-TFE | H | CH2CF3 | | 2C-TFM | H | CF3 | | 2C-YN | H | C≡CH | | 2C-V | H | CH=CH2 |
LegalityCanadaAs of October 12, 2016, the 2C-x family of substituted phenethylamines is a controlled substances (Schedule III) in Canada.[6] See also- Substituted phenethylamines
- Substituted amphetamines
- Substituted methylenedioxyphenethylamines
- DOx, 3Cs, 25-NB
- Substituted tryptamines
References 1. ^Alexander Shulgin, Tania Manning and Paul F Daley. The Shulgin Index. Volume 1. Psychedelic Phenethylamines and Related Compounds. Transform Press, 2011. {{ISBN|978-0-9630096-3-0}}
2. ^Daniel Trachsel, David Lehmann and Christoph Enzensperger. Phenethylamine Von der Struktur zur Funktion, pp 762-810. Nachtschatten Verlag AG, 2013. {{ISBN|978-3-03788-700-4}}
3. ^{{CitePiHKAL}}
4. ^1 2 3 4 5 6 {{cite web|title=Shulgin’s Sulfur Symphony – Part I|url=http://countyourculture.com/2011/01/15/shulgins-sulfur-symphony-part-i/|website=countyourculture|date=15 January 2011}}
5. ^1 2 3 4 5 6 7 8 9 10 11 12 13 {{cite web|title=Shulgin’s Sulfur Symphony – Part I|url=http://countyourculture.com/2011/01/15/shulgins-sulfur-symphony-part-i/|website=countyourculture|date=15 January 2011}}
6. ^{{Cite web |title=Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines) |url=http://gazette.gc.ca/rp-pr/p2/2016/2016-05-04/html/sor-dors72-eng.php |work=Canada Gazette |volume=150 |issue=9 |date=April 15, 2016 |access-date=August 28, 2016}}
{{2C's}}{{Hallucinogens}}{{Serotonergics}}{{TAAR ligands}}{{Phenethylamines}}{{DEFAULTSORT:2c (Psychedelics)}} 1 : Chemical classes of psychoactive drugs |