4,5,6-Trimethoxytryptamine

Base Information

Chemical Name:4,5,6-Trimethoxytryptamine
CAS No.:5376-34-1
Molecular Formula:C13H19ClN2O3
Molecular Weight:286.7546
Hs Code.:
Mol file:5376-34-1.mol

Synonyms:4,5,6-Trimethoxytryptamine;3-(2-Aminoethyl)-4,5,6-trimethoxyindole;5376-34-1;INDOLE, 3-(2-AMINOETHYL)-4,5,6-TRIMETHOXY-, HYDROCHLORIDE;C13H18N2O3.ClH;1H-Indole-3-ethanamine, 4,5,6-trimethoxy-;LS-82302;2-(4,5,6-trimethoxy-1H-indol-3-yl)ethylazanium;chloride

Suppliers and Price of 4,5,6-Trimethoxytryptamine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 4,5,6-Trimethoxytryptamine

Chemical Property:

Vapor Pressure:2.18E-07mmHg at 25°C
Boiling Point:423.7°Cat760mmHg
Flash Point:210.1°C
Density:g/cm³
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:286.1084202
Heavy Atom Count:19
Complexity:265

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C(=C2C(=C1)NC=C2CC[NH3+])OC)OC.[Cl-]

Technology Process of 4,5,6-Trimethoxytryptamine

There total 1 articles about 4,5,6-Trimethoxytryptamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 5376-34-1
2-(4,5,6-trimethoxy-indol-3-yl)-ethylamine

Guidance literature:: DOI:10.1002/hlca.19630460418

Reference yield:

: 119-61-9
benzophenone

: 5376-34-1
2-(4,5,6-trimethoxy-indol-3-yl)-ethylamine

: 4,5,6-trimethoxy-3-<2-(diphenylmethanamino)-ethyl>-indole hydrochloride

Guidance literature:: With hydrogenchloride; sodium tetrahydroborate; boron trifluoride diethyl etherate; Yield given. Multistep reaction; 1.) 130 deg C, 30 min; 2.) methanol, room temp.;