Exploring 2C-TFM. To explore a different substance…

Names:
2C-TFM · 2C-CF3 · 4-Trifuouromethyl-2,5-dimethoxyphenethylamine
IUPAC name:
2-[2,5-Dimethoxy-4-(trifluoromethyl)phenyl]ethan-1-amine
ID: 2040 · Formula: C11H14F3NO2 · Molecular weight: 249.23
InChI: InChI=1S/C11H14F3NO2/c1-16-9-6-8(11(12,13)14)10(17-2)5-7(9)3-4-15/h5-6H,3-4,15H2,1-2H3

Trachsel, D. Fluorine in psychedelic phenethylamines. Drug Test. Analysis, 1 Jul 2012, 4 (7-8), 577-590. 1.0 MB. http://dx.doi.org/10.1002/dta.413

Leth-Petersen, S; Bundgaard, C; Hansen, M; Carnerup, MA; Kehler, J; Kristensen, JL. Correlating the metabolic stability of psychedelic 5-HT2A agonists with anecdotal reports of human oral bioavailability. Neurochem. Res., 12 Feb 2014, 39 (10), 2018-2023. 625 kB. http://dx.doi.org/10.1007/s11064-014-1253-y

Nichols, DE; Frescas, SP; Marona-Lewicka, D; Huang, X; Roth, BL; Gudelsky, GA; Nash, JF. 1-(2,5-Dimethoxy-4-(trifluoromethyl)phenyl)-2-aminopropane: A potent serotonin 5-HT2A/2C agonist. J. Med. Chem., 1 Jan 1994, 37 (25), 4346–4351. 873 kB. http://dx.doi.org/10.1021/jm00051a011

Parrish, JC; Braden, MR; Gundy, E; Nichols, DE. Differential phospholipase C activation by phenylalkylamine serotonin 5-HT2A receptor agonists. J. Neurochem., 1 Dec 2005, 95 (6), 1575–1584. 301 kB. http://dx.doi.org/10.1111/j.1471-4159.2005.03477.x

Parrish, JC. Toward a molecular understanding of hallucinogen action. Ph. D. Thesis, Purdue University, West Lafayette, IN, 1 Jan 2006. 5.5 MB.

Braden, MR. Towards a biophysical understanding of hallucinogen action. Ph. D. Thesis, Purdue University, West Lafayette, IN, 1 Jan 2007. 8.4 MB.

25TFM-NBOMe
25TFM-NBOH
25TFM-NBF
25TFM-NBMD
DOTFM
2C-B
2C-C
2C-D
2C-E
2C-F
2C-H
2C-I
2C-N
2C-O-4
2C-P
2C-SE
2C-T
2C-T-2
2C-T-4
2C-T-7
2C-T-8
2C-T-9
2C-T-13
2C-T-15
2C-T-17
2C-T-21
TMPEA
2C-CN
2C-CA · 2C-COOH
2C-O-2
2C-O-7
2C-O-19
2C-SE-2
2C-SE-4
2C-SE-7
2C-SE-21
2C-TE
2C-T-10
2C-T-11
2C-T-12
2C-T-14
2C-T-5
2C-T-16
2C-T-6
2C-T-19
2C-T-21.5
2C-T-22
2C-T-18
2C-T-23
2C-YN
2C-pEtOH
2C-pKet
2C-T-3
2C-T-25
2C-T-27
2C-T-28
2C-T-30
2C-T-31
2C-T-32
2C-T-33
2C-VI
2C-BI-1
2C-BI-2
2C-BI-3
2C-BI-4
2C-BI-5
2C-BI-6
2C-BI-7
2C-BI-8
2C-BI-9
2C-BI-10
2C-BI-11
2C-BI-12
2326
2324
2327
2C-IP
2C-EF
2C-NH
2C-HM
2C-IB
2C-TFE
2C-O-22
2C-O-21.5
2C-O-21
2C-A
TFMBOX
25TFM-NBOMe
25TFM-NBOH
25TFM-NBF
25TFM-NBMD
DOTFM
2C-B
2C-C
2C-D
2C-E
2C-F
2C-H
2C-I
2C-N
2C-O-4
2C-P
2C-SE
2C-T
2C-T-2
2C-T-4
2C-T-7
2C-T-8
2C-T-9
2C-T-13
2C-T-15
2C-T-17
2C-T-21
TMPEA
2C-CN
2C-CA · 2C-COOH
2C-O-2
2C-O-7
2C-O-19
2C-SE-2
2C-SE-4
2C-SE-7
2C-SE-21
2C-TE
2C-T-10
2C-T-11
2C-T-12
2C-T-14
2C-T-5
2C-T-16
2C-T-6
2C-T-19
2C-T-21.5
2C-T-22
2C-T-18
2C-T-23
2C-YN
2C-pEtOH
2C-pKet
2C-T-3
2C-T-25
2C-T-27
2C-T-28
2C-T-30
2C-T-31
2C-T-32
2C-T-33
2C-VI
2C-BI-1
2C-BI-2
2C-BI-3
2C-BI-4
2C-BI-5
2C-BI-6
2C-BI-7
2C-BI-8
2C-BI-9
2C-BI-10
2C-BI-11
2C-BI-12
2326
2324
2327
2C-IP
2C-EF
2C-NH
2C-HM
2C-IB
2C-TFE
2C-O-22
2C-O-21.5
2C-O-21
2C-A
TFMBOX
11 December 2017 · Creative Commons BY-NC-SA ·