| Systematic (IUPAC) name | |
|---|---|
| 2-(4-chloro-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | Class C (NZ) |
| Identifiers | |
| CAS number | 1227608-02-7 |
| ATC code | ? |
| PubChem | CID 46856354 |
| ChemSpider | 24583389 |
| Chemical data | |
| Formula | C18H22ClNO3 |
| Mol. mass | 335.824 g/mol |
| SMILES | eMolecules & PubChem |
|
|
| |
|
2C-C-NBOMe (NBOMe-2C-C, 25C-NBOMe, Cimbi-82, Pandora, Dime) is a derivative of the phenethylamine hallucinogen 2C-C, which acts as a potent partial agonist for the 5HT2A receptor, and has been studied in its 11C radiolabelled form as a potential ligand for mapping the distribution of 5-HT2A receptors in the brain, using positron emission tomography (PET).[1] Anecdotal reports from human users suggest 2C-C-NBOMe to be an active hallucinogen at a dose of as little as 200-500mcg insufflated, making it only slightly less potent than LSD.[citation needed] It was discovered to be on sale as a designer drug in New Zealand in early 2012, but was withdrawn from sale after a statement by Associate Health Minister Peter Dunne that 25C-NBOMe would be considered to be substantially similar in chemical structure to the illegal hallucinogen DOB, and therefore a Class C controlled drug analogue.[2][3][4]
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| This psychedelics, dissociatives and deliriants-related article is a stub. You can help Wikipedia by expanding it. |
This entry is from Wikipedia, the leading user-contributed encyclopedia. It may not have been reviewed by professional editors (see full disclaimer)