Acetamide, N-(2-(indol-3-YL)ethyl)thio-

Base Information

Chemical Name:Acetamide, N-(2-(indol-3-YL)ethyl)thio-
CAS No.:10022-74-9
Molecular Formula:C12H14 N2 S
Molecular Weight:218.318
Hs Code.:
DSSTox Substance ID:DTXSID60143028
Nikkaji Number:J554.953A
Mol file:10022-74-9.mol

Synonyms:N-Thioacetyltryptamine;N-(2-(3-Indolyl)ethyl)thioacetamide;BRN 0396218;10022-74-9;ACETAMIDE, N-(2-(INDOL-3-YL)ETHYL)THIO-;N-(2-(1H-Indol-3-yl)ethyl)ethanethioamide;ACETAMIDE,N-(2-(INDOL-3-YL)ETHYL)THIO-;Ethanethioamide, N-(2-(1H-indol-3-yl)ethyl)-;5-22-10-00076 (Beilstein Handbook Reference);DTXSID60143028;LS-9787;N-(Thioacetyl)-1H-indole-3-(ethanamine)

Suppliers and Price of Acetamide, N-(2-(indol-3-YL)ethyl)thio-

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 6 raw suppliers

Chemical Property of Acetamide, N-(2-(indol-3-YL)ethyl)thio-

Chemical Property:

Vapor Pressure:8.86E-07mmHg at 25°C
Boiling Point:405.3°Cat760mmHg
Flash Point:198.9°C
Density:1.202g/cm³
XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:218.08776963
Heavy Atom Count:15
Complexity:230

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=S)NCCC1=CNC2=CC=CC=C21

Technology Process of Acetamide, N-(2-(indol-3-YL)ethyl)thio-

There total 2 articles about Acetamide, N-(2-(indol-3-YL)ethyl)thio- 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: 95.0%

: 1016-47-3
N-Acetyltryptamine

: 10022-74-9
N-(thioacetyl)tryptamine

Guidance literature:: With Lawessons reagent; In 1,2-dimethoxyethane; for 3h; Ambient temperature;
DOI:10.1248/cpb.33.3237

Reference yield:

: 10022-74-9
N-(thioacetyl)tryptamine

Guidance literature:: Tryptamin, Dithioessigsaeure-ethylester, Me.;

Reference yield:

: 10022-74-9
N-(thioacetyl)tryptamine

: 61-53-0
5-fluoro-α-methyltryptamine

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / acetonitrile / 4 h / Ambient temperature

2: 86 percent / NaBH₄ / methanol / 1 h / -78 °C

With sodium tetrahydroborate; In methanol; acetonitrile;
DOI:10.1248/cpb.33.3237