| Width | 215px |
|---|---|
| Legal status | In general unscheduled |
| Class | Serotonin receptor modulator; Serotonergic psychedelic; Hallucinogen |
| Atc prefix | None |
| Cas number | 100939-87-5 |
| Unii | 9AF4JQU2FM |
| Chembl | 348140 |
| Pubchem | 4738744 |
| Chemspiderid | 3925965 |
| Synonyms | 2C-B-PP |
| Iupac name | 1-(2,5-dimethoxy-4-bromophenyl)piperazine |
| C | 12 |
| H | 17 |
| Br | 1 |
| N | 2 |
| O | 2 |
| Smiles | COC1=CC(=C(C=C1N2CCNCC2)OC)Br |
| Stdinchi | 1S/C12H17BrN2O2/c1-16-11-8-10(12(17-2)7-9(11)13)15-5-3-14-4-6-15/h7-8,14H,3-6H2,1-2H3 |
| Stdinchikey | JLAQUWGWRNMYGA-UHFFFAOYSA-N |
2C-B-PP, also known as 2,5-dimethoxy-4-bromophenylpiperazine, is a psychedelic drug of the phenylpiperazine family. It acts as an agonist at serotonin receptors, and in studies on rats substituted for DOM with around 10-fold lower potency but similar rates of stimulus-appropriate responding at the highest dose.[1][2]: 867–868
See also
- 2C-B-BZP
- 2C-B-3PIP
- 2C-B-aminorex
- 2C-B-morpholine
- 3-Chloro-4-fluorophenylpiperazine
- CPD-1
- ORG-12962
- Quipazine
- Substituted piperazine
References
- ^ Lyon RA, Titeler M, McKenney JD, Magee PS, Glennon RA (May 1986). "Synthesis and evaluation of phenyl- and benzoylpiperazines as potential serotonergic agents". Journal of Medicinal Chemistry. 29 (5): 630–634. doi:10.1021/jm00155a008. PMID 3701781
- ^ Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine: Von der Struktur zur Funktion. Nachtschatten Verlag AG. ISBN 978-3-03788-700-4.