Indole, 3-(2-(methylamino)ethyl)-5-methylthio-

Base Information

Chemical Name:Indole, 3-(2-(methylamino)ethyl)-5-methylthio-
CAS No.:5564-19-2
Molecular Formula:C12H16N2S
Molecular Weight:220.3338
Hs Code.:
DSSTox Substance ID:DTXSID50204172

Synonyms:BRN 0394069;INDOLE, 3-(2-(METHYLAMINO)ETHYL)-5-METHYLTHIO-;5564-19-2;3-(2-N-Methylaminoethyl)-5-methylthioindole;5-22-12-00065 (Beilstein Handbook Reference);DTXSID50204172;LS-83253

Suppliers and Price of Indole, 3-(2-(methylamino)ethyl)-5-methylthio-

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

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Chemical Property of Indole, 3-(2-(methylamino)ethyl)-5-methylthio-

Chemical Property:

Vapor Pressure:8.89E-07mmHg at 25°C
Boiling Point:405.3°Cat760mmHg
Flash Point:198.9°C
Density:1.15g/cm³
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:220.10341969
Heavy Atom Count:15
Complexity:198

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CNCCC1=CNC2=C1C=C(C=C2)SC

Technology Process of Indole, 3-(2-(methylamino)ethyl)-5-methylthio-

There total 3 articles about Indole, 3-(2-(methylamino)ethyl)-5-methylthio- 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:

: N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)-2-oxo-acetamide

: 5564-19-2
N-methyl-5-methylthiotryptamine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 72h; Heating;

Reference yield:

: 77248-65-8
5-methylthio-1H-indole

: 5564-19-2
N-methyl-5-methylthiotryptamine

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / diethyl ether; tetrahydrofuran / 1 h / 20 °C

2: 80 percent / H₂O

3: LiAlH₄ / tetrahydrofuran / 72 h / Heating

With lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; water;

Reference yield:

: 228098-50-8
5-methylthio-indol-3-ylglyoxyloyl chloride

: 5564-19-2
N-methyl-5-methylthiotryptamine

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / H₂O

2: LiAlH₄ / tetrahydrofuran / 72 h / Heating

With lithium aluminium tetrahydride; In tetrahydrofuran; water;