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Names

5,6-MDAT
2-Amino-5,6-methylenedioxytetralin

IUPAC names

6,7,8,9-Tetrahydro-2H-naphtho[1,2-d][1,3]dioxol-7-amine
6,7,8,9-Tetrahydronaphtho[1,2-d][1,3]dioxol-7-amine

ID 404 · Formula C₁₁H₁₃NO₂ · Molecular weight 191.226

InChI InChI=1S/C11H13NO2/c12-8-2-3-9-7(5-8)1-4-10-11(9)14-6-13-10/h1,4,8H,2-3,5-6,12H2

InChI Key RIOMIXSSVKANQH-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES N[C@H]1CCc2c(C1)ccc1c2OCO1

ChemSpider 23232170
PubChem 44375355

Shulgin Index See #77 MDA · Table 5Page 338Row 27

Phenethylamine: Von der Strucktur zur Funktion 5,6-MDAT: 7.5 (102) 596

Nichols, DE; Brewster, WK; Johnson, MP; Oberlender, R; Riggs, RM. Nonneurotoxic tetralin and indan analogues of 3,4-(methylenedioxy)amphetamine (MDA). J. Med. Chem., 1 Feb 1990, 33 (2), 703–710. 1.1 MB. https://doi.org/10.1021/jm00164a037

Nichols, DE; Oberlender, R. Structure-activity relationships of MDMA-like substances. In Pharmacology and Toxicology of Amphetamine and Related Designer Drugs. NIDA Research Monograph 94; Asghar, K; De Souza, E, Eds., U.S. Department of Health and Human Services, National Institute of Health, U.S. Government Printing Office, Washington, DC, 1 Jan 1989; pp 1-29. 282 kB.

Nichols, DF; Oberlender, R. Structure-activity relationships of MDMA and related compounds: A new class of psychoactive agents? In Ecstasy: The Clinical, Pharmacological and Neurotoxicological Effects of the Drug MDMA; Peroutka, SJ, Ed., Springer US, 1 Jan 1990; pp 105–131. 733 kB. https://doi.org/10.1007/978-1-4613-1485-1_7 #19

Oberlender, RA. Stereoselective aspects of hallucinogenic drug action and drug discrimination studies of entactogens. Ph. D. Thesis, Purdue University, West Lafayette, IN, 1 May 1989. 8.2 MB. #5,6-MDAT MS,NMR,IR,other

5,6-MDMAI · MDMAI

6,7-MDAT

4,5-MDMAI

2464

DMHH-2

MDMH-4

Hydrohydrastinine · MDHM-4

10185

10208

1821

5-Methoxytryptophol

Fenmetramide

Dehydrolemaireocereine

Pycnarrhine

2,5-DMeA NS · 2,5-Dimethyl-β-methyl-β-nitrostyrene

7 Dec 2019 · · Isomer Design