Alle Fotos(1)
Wichtige Dokumente
560529
3,4-Methylendioxyphenethylamin -hydrochlorid
98%
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
Größe auswählen
Ansicht ändern
1 G
54,00 €
5 G
205,00 €
About This Item
Empirische Formel (Hill-System):
C9H11NO2 · HCl
CAS-Nummer:
Molekulargewicht:
201.65
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
![[Pd(OAc)2]3 reagent grade, 98%](/deepweb/assets/sigmaaldrich/product/structures/508/249/99a0ef2c-b77c-4d73-8ed9-0cca05b6b41f/640/99a0ef2c-b77c-4d73-8ed9-0cca05b6b41f.png)
Qualitätsniveau
Assay
98%
mp (Schmelzpunkt)
216-218 °C (lit.)
Funktionelle Gruppe
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
InChIKey
NDYXFQODWGEGNU-UHFFFAOYSA-N
Allgemeine Beschreibung
3,4-Methylenedioxyphenethylamine hydrochloride can be synthesized by reacting aluminum chloride, LiAlH4 and 3,4-methylenedioxyphenylacetonitrile.[1]
Anwendung
3,4-Methylenedioxyphenethylamine hydrochloride may be used to synthesize N-(3,4-methylenedioxyphenethyl)-2-(3-bromo-4-methoxyphenyl)acetamide.[2]
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
Hier finden Sie alle aktuellen Versionen:
Besitzen Sie dieses Produkt bereits?
In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.
Kunden haben sich ebenfalls angesehen
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
D J De Silva et al.
Neuroscience, 134(4), 1363-1375 (2005-08-02)
Substituted amphetamines such as p-chloroamphetamine and the abused drug methylenedioxymethamphetamine cause selective destruction of serotonin axons in rats, by unknown mechanisms. Since some serotonin neurones also express neuronal nitric oxide synthase, which has been implicated in neurotoxicity, the present study
Jan G Bruhn et al.
Journal of psychoactive drugs, 40(2), 219-222 (2008-08-30)
Human interest in psychoactive phenethylamines is known from the use of mescaline-containing cacti and designer drugs such as Ecstasy. From the alkaloid composition of cacti we hypothesized that substances resembling Ecstasy might occur naturally. In this article we show that
An aryne route to laureline, and related topics.
Gibson MS, et al.
J. Chem. Soc. Sect. C, 16, 2234-2238 (1970)
Aktive Filter
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
Setzen Sie sich mit dem technischen Dienst in Verbindung.
