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formaldehyd
2-(5-methoxy-2-methyl-1H-indol-3-yl)ethan-1-amine hydrochloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With sodium methylate; sodium cyanoborohydride; acetic acid In methanol; water | 80% |
N,N-dimethyl-4-oxopentanamine hydrochloride
4-methoxyphenylhydrazine hydrochloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-4-oxopentanamine hydrochloride; 4-methoxyphenylhydrazine hydrochloride With sulfuric acid; acetic acid at 40 - 60℃; for 3.5 - 4.5h; Heating / reflux; Stage #2: With sodium carbonate In water pH=10; | 78.2% |
(5-methoxy-2-methyl-indol-3-yl)-acetic acid dimethylamide
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
2-(5-Methoxy-2-methyl-1H-indol-3-yl)-N,N-dimethyl-2-oxo-acetamide
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
5-methoxy-2-methyl-1H-indole
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: diethyl ether 2: H2O; CHCl3 3: LiAlH4 View Scheme |
2-(5-methoxy-2-methyl-1H-indol-3-yl)-2-oxoacetyl chloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2O; CHCl3 2: LiAlH4 View Scheme |
5-Methoxy-2-methylindole-3-acetic acid
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 195 °C 2: LiAlH4; diethyl ether View Scheme |
2-(5-methoxy-2-methyl-1H-indol-3-yl)ethan-1-amine hydrochloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With sodium hydroxide; formaldehyd; sodium methylate; sodium cyanoborohydride; acetic acid In methanol | 1.215 g (80%) |
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
methyl iodide
Conditions | Yield |
---|---|
Multistep reaction.; | 16% |
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
benzenesulfonyl chloride
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydrogensulfate In dichloromethane at 20℃; for 0.333333h; |
Empirical Formula: C14H20N2O
Molecular Weight: 232.3214 g/mol
Index of Refraction: 1.589
Density: 1.079 g/cm3
Flash Point: 185.8 °C
Enthalpy of Vaporization: 63.23 kJ/mol
Boiling Point: 383.7 °C at 760 mmHg
Vapour Pressure: 4.32E-06 mmHg at 25 °C
Structure of Methyl-2-methoxy-5-N-dimethyltryptamine (CAS NO.67292-68-6):
IUPAC Name: 2-(5-Methoxy-2-methyl-1H-indol-3-yl)-N,N-dimethylethanamine
Methyl-2-methoxy-5-N-dimethyltryptamine (CAS NO.67292-68-6) is a psychoactive drug of the tryptamine chemical class which acts as a psychedelic, and is also interfering with binding to and/or activation of the serotonin 5-HT2A receptor.
1. | ipr-rat LD50:74 mg/kg | BSCFAS Bulletin de la Societe Chimique de France.(5)(1965),1411. | ||
2. | ipr-mus LD50:100 mg/kg | BSCFAS Bulletin de la Societe Chimique de France.(5)(1965),1411. | ||
3. | ivn-mus LD50:48 mg/kg | BSCFAS Bulletin de la Societe Chimique de France.(5)(1965),1411. | ||
4. | ivn-rbt LD50:22 mg/kg | BSCFAS Bulletin de la Societe Chimique de France.(5)(1965),1411. |
Poison by intraperitoneal and intravenous routes. When heated to decomposition it emits toxic fumes of NOx.
Methyl-2-methoxy-5-N-dimethyltryptamine ,its cas register number is 67292-68-6. It also can be called 5-MeO-TMT ; and Indole, 3-(2-(dimethylamino)ethyl)-5-methoxy-2-methyl- . Methyl-2-methoxy-5-N-dimethyltryptamine (CAS NO.67292-68-6) was first synthesized by Alexander Shulgin and reported in his book TiHKAL and is claimed to show psychoactive effects at a dosage of 75-150 mg orally, but these are relatively mild compared to those of other similar compounds.