CT-5172
| File:CT-5172.svg | |
| Clinical data | |
|---|---|
| Other names | CT5172; 2,6-Dimethoxy-3,5-dichlorophenethylamine |
| Drug class | Serotonergic psychedelic; Hallucinogen |
| ATC code |
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| Identifiers | |
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| E number | {{#property:P628}} |
| CompTox Dashboard (EPA) |
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| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C10H13Cl2NO2 |
| Molar mass | 250.12 g·mol−1 |
| 3D model (JSmol) | |
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CT-5172, also known as 2,6-dimethoxy-3,5-dichlorophenethylamine, is a claimed hallucinogen of the phenethylamine family.[1][2][3] It is an analogue of the serotonergic psychedelics mescaline and the 2C series but with an unusual substitution pattern on the benzene ring that includes methoxy groups at the 2 and 6 positions and chlorine atoms at the 3 and 5 positions.[1][2][3] The drug was reported to have significant but relatively weak mescaline-like effects in cats.[1][3] CT-5172 was first described in the scientific literature by 1969.[2][3] Various related analogues, such as CT-5126 and CT-4719, have also been described.[1][2][3] CT-5172 and related compounds were developed at the Laboratoire de Chimie Thérapeutique (CT; Therapeutic Chemistry Laboratory) of the Pasteur Institute in Paris, France.[1][2][3]
See also
[edit | edit source]- Substituted methoxyphenethylamine
- Ψ-2C-T-4 (2,6-dimethoxy-4-isopropylthiophenethylamine)
- ψ-DOM (2,6-dimethoxy-4-methylamphetamine)
- TMA-6 (2,4,6-trimethoxyamphetamine)
- 2-Bromomescaline
- DODC (2,5-dimethoxy-3,4-dichloroamphetamine)
References
[edit | edit source]- ^ a b c d e Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ a b c d e Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ a b c d e f Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
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