Exploring 4C-H. To explore a different substance…

Names:
4C-DMA
4C-H
1-(2,5-Dimethoxyphenyl)-2-aminobutane
IUPAC name:
1-(2,5-Dimethoxyphenyl)butan-2-amine
183 · C12H19NO2 · 209.285
InChI=1S/C12H19NO2/c1-4-10(13)7-9-8-11(14-2)5-6-12(9)15-3/h5-6,8,10H,4,7,13H2,1-3H3
BGWUWDWDTLZQAZ-UHFFFAOYSA-N This stereoisomer Any stereoisomer

Standridge, RT; Howell, HG; Tilson, HA; Chamberlain, JH; Holava, HM; Gylys, JA; Partyka, RA; Shulgin, AT. Phenylalkylamines with potential psychotherapeutic utility. 2. Nuclear substituted 2-amino-1-phenylbutanes. J. Med. Chem., 1 Jan 1980, 23 (2), 154–162. 1.1 MB. https://doi.org/10.1021/jm00176a010

Partyka, RA; Standridge, RT; Howell, HG; Shulgin, AT. 2-Amino-1-(2,5-dimethoxyphenyl)butanes. U.S. Patent 4,105,695, 8 Aug 1978. 645 kB.

2C-E
2C-G
DOM
ψ-DOM
2,5-DMMA · METHYL-DMA
4C-DMPEA
N-Me-2C-D
2C-D-2-EtO · 2CD-2ETO
2C-D-5-EtO · 2CD-5ETO
m-DOM · 5-DOM
o-DOM · 2-DOM
6-Me-2,4-DOM · Z-7.1
2,4-DMMA
ψ-2C-E
4-Propoxynorephedrine
homo-DMA
homo-N-Me-2,5-DMPEA
BO3MDM
BO3MEA
BO3EE
BO3P
N,N-Me-DMPEA-2
N-Me-2,3-DMA
N-Me-2,3-EMPEA
4C-2,4-DMPEA
2,4-DEPEA
N-Me,N-iPr-DHPEA
N-Bu-DHPEA
N-iBu-DHPEA
MHEA
N-Me-α-Et-GEA
Salicifoline
HMEA
N,N-Me-DMPEA
N-Et-DMPEA
DMMA
N-Me-EMPEA
EMA
MEA
DEPEA
β-HO-N-Me-2-M-5-MeA
N,N-Me-2,5-HMA
N,N-Me-2,5-DMPEA
β,N-Me-2,5-DMPEA
N,N-Me-3,5-DMPEA
N-Me-3,5-DMA
N,N-Me-2,6-DMPEA
N-Me-2,6-DMA
4-Me-2,3-DOM
3-Me-2,4-DOM
2-Me-3,4-DOM
5-Me-2,3-DOM
3-DOM
2-Me-3,5-DOM
BMD
5-Me-3,4-DOM
4-Me-3,5-DOM
6-Me-2,3-DOM
3-Me-2,6-DOM
2-Me-3,6-DOM
6-Me-2,4-EMPEA
2C-H-2-iPrO
10432
10408
DE
10096
10048
10034
10027
3,5-DMB
2C-H-5-iPrO
19 September 2018 · Creative Commons BY-NC-SA ·