Indole, 5-(dimethylamino)-

Base Information

Chemical Name:Indole, 5-(dimethylamino)-
CAS No.:6843-23-8
Molecular Formula:C10H12N2
Molecular Weight:160.2157
Hs Code.:
DSSTox Substance ID:DTXSID60218548
Wikidata:Q83095425
Mol file:6843-23-8.mol

Synonyms:N,N-dimethyl-1H-indol-5-amine;6843-23-8;INDOLE, 5-(DIMETHYLAMINO)-;5-(Dimethylamino)indole;BRN 0386931;5-22-10-00012 (Beilstein Handbook Reference);1H-Indol-5-amine, N,N-dimethyl-;5-dimethylaminoindole;SCHEMBL3335239;DTXSID60218548;(1H-Indol-5-yl)-dimethyl-amine;AKOS022844945;LS-82922

Suppliers and Price of Indole, 5-(dimethylamino)-

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

American Custom Chemicals Corporation
N,N-DIMETHYL-1H-INDOL-5-AMINE 95.00%
5MG
$ 501.75

AccelPharmtech
N,N-dimethyl-1H-Indol-5-amine 97.00%
25G
$ 9900.00

AccelPharmtech
N,N-dimethyl-1H-Indol-5-amine 97.00%
5G
$ 5270.00

AccelPharmtech
N,N-dimethyl-1H-Indol-5-amine 97.00%
1G
$ 3060.00

Total 6 raw suppliers

Chemical Property of Indole, 5-(dimethylamino)-

Chemical Property:

Vapor Pressure:0.000495mmHg at 25°C
Boiling Point:313.5°Cat760mmHg
PKA:17.37±0.30(Predicted)
Flash Point:143.4°C
PSA：19.03000
Density:1.145g/cm³
LogP:2.23390
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:160.100048391
Heavy Atom Count:12
Complexity:156

Purity/Quality:

97% ^*data from raw suppliers

N,N-DIMETHYL-1H-INDOL-5-AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C1=CC2=C(C=C1)NC=C2

Technology Process of Indole, 5-(dimethylamino)-

There total 3 articles about Indole, 5-(dimethylamino)- 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: 76.0%

: 6844-32-2
5-indolyltrimethylammonium chloride

: 6843-23-8
5-(N,N-dimethylamino)indole

Guidance literature:: 5-indolyltrimethylammonium chloride; With sodium; In propan-1-ol; for 17h; Reflux;

With water; In diethyl ether;

Reference yield: 40.0%

: 6843-23-8
5-(N,N-dimethylamino)indole

Guidance literature:: With potassium fluoride; bis(pinacol)diborane; In ethanol; at 100 ℃; for 12h; Inert atmosphere;

Reference yield:

: 6884-83-9
5-indolyltrimethylammonium picrate

: 6843-23-8
5-(N,N-dimethylamino)indole

Guidance literature:: Multi-step reaction with 2 steps

1: Dowex 2 resin (chloride) / methanol / 17 h / 20 °C

2: sodium / propan-1-ol / 17 h / Reflux

With sodium; In methanol; propan-1-ol;