Indole, 3-(2-amino-2-methylpropyl)-5-bromo-

Base Information

Chemical Name:Indole, 3-(2-amino-2-methylpropyl)-5-bromo-
CAS No.:833-04-5
Molecular Formula:C12H15BrN2
Molecular Weight:267.1649
Hs Code.:
DSSTox Substance ID:DTXSID30232251
Wikidata:Q83113286

Synonyms:833-04-5;BRN 5518967;INDOLE, 3-(2-AMINO-2-METHYLPROPYL)-5-BROMO-;5-Bromo-alpha,alpha-dimethyltryptamine;C12H15BrN2;1-(5-bromo-1H-indol-3-yl)-2-methylpropan-2-amine;SCHEMBL10940983;C12-H15-Br-N2;DTXSID30232251;IMBZTQWJYSRGPS-UHFFFAOYSA-N;AB09841;LS-82315;2-(5-bromo 3-indolyl)1,1-dimethyl ethylamine;EN300-6729877;5-bromo-alpha,alpha-dimethyl-1H-indol-3-yl-ethaneamine;2-(5-BROMO-1H-INDOL-3-YL)-1,1-DIMETHYL-ETHYLAMINE

Suppliers and Price of Indole, 3-(2-amino-2-methylpropyl)-5-bromo-

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 1 raw suppliers

Chemical Property of Indole, 3-(2-amino-2-methylpropyl)-5-bromo-

Chemical Property:

Vapor Pressure:1.4E-06mmHg at 25°C
Boiling Point:399.1°Cat760mmHg
Flash Point:195.2°C
Density:1.423g/cm³
XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:266.04186
Heavy Atom Count:15
Complexity:230

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(CC1=CNC2=C1C=C(C=C2)Br)N

Technology Process of Indole, 3-(2-amino-2-methylpropyl)-5-bromo-

There total 3 articles about Indole, 3-(2-amino-2-methylpropyl)-5-bromo- 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: 99.0%

: 837-87-6
5-bromo-3-(2,2-dimethyl-2-nitroethyl)-1H-indole

: 833-04-5
5-bromo-α,α,2-trimethyl-1H-indole-3-ethanamine

Guidance literature:: With nickel; hydrazine hydrate; In ethanol; for 2h; Heating;
DOI:10.1021/jm00177a015

Reference yield:

: 830-93-3
N-[(5-bromo-1H-indol-3-yl)methyl]-N,N-dimethylamine

: 833-04-5
5-bromo-α,α,2-trimethyl-1H-indole-3-ethanamine

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / NaOH / 18 h / Heating

2: 99 percent / 85percent hydrazine hydrate, Raney nickel / ethanol / 2 h / Heating

With sodium hydroxide; nickel; hydrazine hydrate; In ethanol;
DOI:10.1021/jm00177a015