Exploring 3C-P. To explore a different substance…

Names:
3C-P
3,5-Dimethoxy-4-n-propoxyamphetamine
IUPAC name:
1-(3,5-Dimethoxy-4-propoxyphenyl)propan-2-amine
2044 · C14H23NO3 · 253.337
InChI=1S/C14H23NO3/c1-5-6-18-14-12(16-3)8-11(7-10(2)15)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3
KKMCHCCXGKYEKJ-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Trachsel, D. Synthesis of novel (phenylalkyl)amines for the investigation of structure-activity relationships. Part 1. Mescalin derivatives. Helv. Chim. Acta, 21 Jun 2002, 85 (9), 3019–3026. 98 kB. https://doi.org/10.1002/1522-2675(200209)85:9<3019::AID-HLCA3019>3.0.CO;2-4 In German.

Leminger, O. Příspěvek k chemii v jádře alkoxylovaných β-fenoetylaminů - II. Chemický průmysl, 1972, 22, 553–557. 581 kB.

McGonigal, MK; Wilhide, JA; Smith, PB; Elliott, NM; Dorman, FL. Analysis of synthetic phenethylamine street drugs using direct sample analysis coupled to accurate mass time of flight mass spectrometry. Forensic Sci. Int., 1 Jun 2017, 275 83–89. 2.3 MB. https://doi.org/10.1016/j.forsciint.2017.02.025 #3C-P

Anon. New drugs in Europe, 2013, European Monitoring Centre for Drugs and Drug Addiction, 1 Jul 2014. 311 kB.

King, LA. New phenethylamines in Europe. Drug Test. Analysis, 1 Jul 2014, 6 (7-8), 808-818. 472 kB. https://doi.org/10.1002/dta.1570

Braun, U; Braun, G; Jacob, P; Nichols, DE; Shulgin, AT. Mescaline Analogs: Substitutions at the 4-Position. In QuaSAR: Quantitative Structure Activity Relationships of Analgesics, Narcotic Antagonists, and Hallucinogens. NIDA Research Monograph 22; Barnett, G; Trsic, M; Willette, RE, Eds., U.S. Department of Health and Human Services, National Institute of Health, U.S. Government Printing Office, Washington, DC, 1978; pp 27–37. 497 kB. Rhodium.

B
EEM
EME
MEE
MPM
TRIS
APM
Hydroxy-DOPR
MIPM
3C-IP
2C-O-19
IB
4C-EtO
β-HO-2,5-DMIPA
β-HO-N-Me-2,5-DEA
I-TRIS
4C-HE
N,N-Me-TMA-2
N-Pr-M
2,4,6-TRIS
SBU · sec-Buscaline
TBU · tert-Buscaline
5983
21 July 2018 · Creative Commons BY-NC-SA ·