Exploring DOM-AI. To explore a different substance…

Names:
DOMAI
DOM-AI
2-Amino-4,7-dimethoxy-5-methylindane
IUPAC name:
4,7-Dimethoxy-5-methyl-2,3-dihydro-1H-inden-2-amine
407 · C12H17NO2 · 207.269
InChI=1S/C12H17NO2/c1-7-4-11(14-2)9-5-8(13)6-10(9)12(7)15-3/h4,8H,5-6,13H2,1-3H3
LBSOVXNUJAVVNS-UHFFFAOYSA-N This stereoisomer Any stereoisomer
COc1cc(C)c(c2c1CC(C2)N)OC

Nichols, DE; Barfknecht, CF; Long, JP; Standridge, RT; Howell, HG; Partyka, RA; Dyer, DC. Potential psychotomimetics. 2. Rigid analogs of 2,5-dimethoxy-4-methylphenylisopropylamine (DOM, STP). J. Med. Chem., 1 Feb 1974, 17 (2), 161–166. 718 kB. https://doi.org/10.1021/jm00248a004

Coutts, RT; Malicky, JL. The synthesis of analogs of the hallucinogen 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM). II. Some ring-methoxylated 1-amino- and 2-aminoindanes. Can. J. Chem., 1 Feb 1974, 52 (3), 381–389. 615 kB. https://doi.org/10.1139/v74-061

Nichols, DE; Weintraub, HJR; Pfister, WR; Yim, GKW. The use of rigid analogues to probe hallucinogen receptors. 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, 1 Jan 1978; pp 70–83. 717 kB. #7

DMCPA
MADAM-6
MDDM
MDE
MDMC
MDMP
METHYL-J · MBDB
F
IDA
α-Pr-MDPEA
2C-G-2
MADAM-2
2C-VI
4-MeO-3-Me-MCAT
5,8-ADT
MeO-B · 4-Methoxybuphedrone
DMA-2-hemiFLY
4-Propoxycathinone
α-Me-N-Pr-MDBA
α,α,N,N-TMMDBA
HMDMA
α-Me-N-iPr-MDBA
BO3A
Hordenine acetate
2,3-MDDMA
2,3-MDE
2,3-MBDB
MAPEA
N-Me-N-Et-MDPEA
N-Pr-MDPEA
N-iPr-MDPEA
α-Et-α-Me-MDPEA
α-iPr-MDPEA
ED-N-DMPEA
DMA-hemiFly-5 · DOH-5-hemiFLY
G-1
M-7
N-Et-ADTN
DMMH-4 · Salsolidine
DMHM-4
2280
1095
1084
1006
10595
736
DV
TMDA
10183
2CH-Ind
Mexedrone
3-MeO-PM
N-Methoxymephedrone
12190
MOMMC
Ethedrone
Dimethedrone
β-homo-MDMA
15 October 2018 · Creative Commons BY-NC-SA ·