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ChemicalBook >> CAS DataBase List >>N,N-Diallyl-5-methoxytryptamine

N,N-Diallyl-5-methoxytryptamine

N,N-Diallyl-5-methoxytryptamine Structure
N,N-Diallyl-5-methoxytryptamine structure
CAS No.
928822-98-4
Chemical Name:
N,N-Diallyl-5-methoxytryptamine
Synonyms
5-MeO-DALT;5-methoxy DALT;5-Methoxy-N,N-dially;N,N-Dially-5-methoxytryptamine;N,N-Diallyl-5-methoxytryptamine;N,N-Diallyl-5-MethoxytryptaMine, GC 95 +%;5-Methoxy-N,N-diallyl-1H-indole-3-ethanamine;5-Methoxy-N,N-di-2-propen-1-yl-1H-indole-3-ethanaMine;5-Methoxy-N,N-diallyl-1H-indole-3-ethanaMine,5-Meo-DALT;1H-Indole-3-ethanamine, 5-methoxy-N,N-di-2-propen-1-yl-
CBNumber:
CB82128739
Molecular Formula:
C17H22N2O
Molecular Weight:
270.37
MDL Number:
MFCD11655942
MOL File:
928822-98-4.mol
Last updated:2023-05-04 17:34:43

N,N-Diallyl-5-methoxytryptamine Properties

Boiling point 422.8±45.0 °C(Predicted)
Density 1.059
solubility DMF: 20 mg/ml; DMF:PBS (pH 7.2) (1:5): 0.15 mg/ml; DMSO: 15 mg/ml; Ethanol: 1.5 mg/ml; Methanol: 1 mg/ml
form A crystalline solid
pka 16.90±0.30(Predicted)
FDA UNII V25VK0QTAA

N,N-Diallyl-5-methoxytryptamine Chemical Properties,Uses,Production

Uses

It is a tryptamine derivative recently used as a component in ‘bath salts’ that act directly on monoamine receptors (similar to MDMA) to produce its psychoactive effects. This compound is a standard for the forensic analysis of samples that may contain this compound.

Uses

N,N-Diallyl-5-methoxytryptamine is a tryptamine derivative recently used as a component in ‘bath salts’ that act directly on monoamine receptors (similar to MDMA) to produce its psychoactive effects. This compound is a standard for the forensic analysis of samples that may contain this compound.

Definition

ChEBI: 1h-indole-3-ethanamine, 5-methoxy-n,n-di-2-propen-1-yl- is a member of tryptamines.

N,N-Diallyl-5-methoxytryptamine Preparation Products And Raw materials

Raw materials

Preparation Products

928822-98-4(N,N-Diallyl-5-methoxytryptamine)Related Search:

2-Methoxyethanol Anisole Allyl chloride Allylthiourea Sodium allylsulfonate
N,N-Diisopropylethylamine Diallylamine p-Anisaldehyde Allyl bromide 4-Methoxyphenol
Diallyldisulfide 4-Methoxybenzylchloride 4-(Trifluoromethoxy)aniline p-Anisidine Allyl glycidyl ether
Diallyl phthalate (Trifluoromethoxy)benzene 5-Methoxytryptamine

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5-Methoxy-N,N-di-2-propen-1-yl-1H-indole-3-ethanaMine 5-Methoxy-N,N-diallyl-1H-indole-3-ethanaMine,5-Meo-DALT N,N-Diallyl-5-MethoxytryptaMine, GC 95 +% 5-Methoxy-N,N-diallyl-1H-indole-3-ethanamine N,N-Diallyl-5-methoxytryptamine 5-MeO-DALT N-allyl-N-(2-(5-methoxy-1H-indol-3-yl)ethyl)prop-2-en-1-amine 5-Methoxy-N,N-dially N,N-Dially-5-methoxytryptamine 5-methoxy DALT N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-prop-2-enylprop-2-en-1-amine 1H-Indole-3-ethanamine, 5-methoxy-N,N-di-2-propen-1-yl- 928822-98-4 Amines Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Research Chemical