2C (psychedelics)
2C (2C-x) is a general name for the family of
amino group.[3]
Nomenclature | R3 | R4 | 2D Structure | CAS number |
---|---|---|---|---|
2C-B | H | Br | 66142-81-2 | |
2C-Bn | H | CH2C6H5
|
||
2C-Bu | H | CH2CH2CH2CH3
|
||
2C-C | H | Cl | 88441-14-9 | |
2C-C-3 [4] | Cl | Cl | ||
2C-CN | H | C≡N
|
88441-07-0 | |
2C-CP | H | C3H5 | ||
2C-D | H | CH3 | 24333-19-5 | |
2C-E | H | CH2CH3 | 71539-34-9 | |
2C-EF | H | CH2CH2F | 1222814-77-8 | |
2C-F | H | F | 207740-15-6 | |
2C-G | CH3 | CH3 | 207740-18-9 | |
2C-G-1
|
CH2 | |||
2C-G-2
|
(CH2)2 | |||
2C-G-3
|
(CH2)3 | 207740-19-0 | ||
2C-G-4
|
(CH2)4 | 952006-59-6 | ||
2C-G-5
|
(CH2)5 | 207740-20-3 | ||
2C-G-6
|
(CH2)6 | |||
2C-G-N
|
(CH)4 | 207740-21-4 | ||
2C-H | H | H | 3600-86-0 | |
2C-I | H | I | 69587-11-7 | |
2C-iP | H | CH(CH3)2
|
1498978-47-4 | |
2C-N | H | NO2 | 261789-00-8 | |
2C-NH2 | H | NH2
|
168699-66-9 | |
2C-PYR | H | Pyrrolidine | ||
2C-PIP | H | Piperidine | ||
2C-O
|
H | OCH3
|
15394-83-9 | |
2C-O-4 | H | OCH(CH3)2 | 952006-65-4 | |
2C-MOM [5] | H | CH2OCH3 | ||
2C-P | H | CH2CH2CH3
|
207740-22-5 | |
2C-Ph | H | C6H5
|
||
2C-Se | H | CH3
|
1189246-68-1 | |
2C-T | H | SCH3
|
61638-09-3 | |
2C-T-2 | H | SCH2CH3 | 207740-24-7 | |
2C-T-3[6] | H | SCH2C(=CH2)CH3 | 648957-40-8 | |
2C-T-4 | H | SCH(CH3)2 | 207740-25-8 | |
2C-T-5[6] | ||||
2C-T-6[6] | ||||
2C-T-7 | H | S(CH2)2CH3 | 207740-26-9 | |
2C-T-8 | H | SCH2CH(CH2)2 | 207740-27-0 | |
2C-T-9[6]
|
207740-28-1 | |||
2C-T-10[6] | ||||
2C-T-11[6] | ||||
2C-T-12[6] | ||||
2C-T-13 | H | S(CH2)2OCH3 | 207740-30-5 | |
2C-T-14[6] | ||||
2C-T-15 | H | SCH(CH2)2 | ||
2C-T-16[7] | H | SCH2CH=CH2 | 648957-42-0 | |
2C-T-17 | H | SCH(CH3)CH2CH3 | 207740-32-7 | |
2C-T-18[6] | ||||
2C-T-19 | H | SCH2CH2CH2CH3 | ||
2C-T-21 | H | S(CH2)2F | 207740-33-8 | |
2C-T-21.5[6] | 648957-46-4 | |||
2C-T-22[6] | 648957-48-6 | |||
2C-T-23[6] | ||||
2C-T-24[6] | ||||
2C-T-25[6] | ||||
2C-T-27[6] | 648957-52-2 | |||
2C-T-28[6] | 648957-54-4 | |||
2C-T-30[6] | ||||
2C-T-31[6] | ||||
2C-T-32[6] | ||||
2C-T-33[6] | ||||
2C-DFM [8]: 770 | H | CHF2 | ||
2C-TFM | H | CF3
|
159277-08-4 | |
2C-TFE | H | CH2CF3 | ||
2C-PFE | H | CF2CF3 | ||
2C-PFS | H | SF5 | ||
2C-YN | H | C≡CH
|
752982-24-4 | |
2C-V | H | CH=CH2 | ||
2C-AL[9] | H | CH2CH=CH2 | ||
2C-B-FLY | Br | 733720-95-1 | ||
2C-B-BUTTERFLY | Br | 502659-24-7 |
Legality
Canada
As of October 12, 2016, the 2C-x family of substituted phenethylamines is a controlled substance (Schedule III) in Canada.[10]
See also
- 25-NB
- Substituted phenethylamines
- Substituted amphetamines
- Substituted methylenedioxyphenethylamines
- DOx
- Substituted tryptamines
- List of miscellaneous 5HT2A agonists
References
- ISBN 978-0-9630096-3-0
- ISBN 978-3-03788-700-4
- OCLC 25627628.
- ^ a b c d e f g h i j k l m n o p q r s t "Shulgin's Sulfur Symphony – Part I". countyourculture. 15 January 2011. Archived from the original on 19 September 2019. Retrieved 22 October 2017.
- .
- ISBN 978-3-03788-700-4.
- ^ Kruegel AC. Phenalkylamines and Methods of Treating Mood Disorders. Patent WO 2022/006186
- ^ "Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)". Canada Gazette. April 15, 2016. Retrieved August 28, 2016.