Quality Level
assay
98%
mp
216-218 °C (lit.)
functional group
amine
SMILES string
Cl.NCCc1ccc2OCOc2c1
InChI
1S/C9H11NO2.ClH/c10-4-3-7-1-2-8-9(5-7)12-6-11-8;/h1-2,5H,3-4,6,10H2;1H
InChI key
NDYXFQODWGEGNU-UHFFFAOYSA-N
General description
3,4-Methylenedioxyphenethylamine hydrochloride can be synthesized by reacting aluminum chloride, LiAlH4 and 3,4-methylenedioxyphenylacetonitrile.
Application
3,4-Methylenedioxyphenethylamine hydrochloride may be used to synthesize N-(3,4-methylenedioxyphenethyl)-2-(3-bromo-4-methoxyphenyl)acetamide.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Milica Ninković et al.
Nephrology (Carlton, Vic.), 13(1), 33-37 (2008-01-18)
The mechanism of MDMA (3,4-methylenedioxymethamphetamine)-induced toxicity is believed to be, in part, due to enhanced oxidative stress. As MDMA is eliminated via the kidney, the aim of this study was to investigate whether MDMA created conditions of oxidative stress within
J F Bagli et al.
Journal of medicinal chemistry, 19(7), 876-882 (1976-07-01)
Synthesis of a series of thienylethanolamines having varying substituents on the thiophene ring and on the nitrogen atom is described using the general procedure reported earlier. In the determination of their pharmacological profile, some of the derivatives showed marked antihypertensive
An aryne route to laureline, and related topics.
Gibson MS, et al.
J. Chem. Soc. Sect. C, 16, 2234-2238 (1970)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 560529-1G | 04061825767147 |
| 560529-5G | 04061832583419 |