2-(4-Iodophenoxy)-N,N,N-trimethylethan-1-aminium iodide

Base Information

Chemical Name:2-(4-Iodophenoxy)-N,N,N-trimethylethan-1-aminium iodide
CAS No.:93790-57-9
Molecular Formula:C₁₁H₁₇INO*I
Molecular Weight:433.071
Hs Code.:
DSSTox Substance ID:DTXSID10546803

Synonyms:93790-57-9;2-(4-Iodophenoxy)-N,N,N-trimethylethan-1-aminium iodide;DTXSID10546803

Suppliers and Price of 2-(4-Iodophenoxy)-N,N,N-trimethylethan-1-aminium iodide

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 0 raw suppliers

Chemical Property of 2-(4-Iodophenoxy)-N,N,N-trimethylethan-1-aminium iodide

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:432.93996
Heavy Atom Count:15
Complexity:159

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[N+](C)(C)CCOC1=CC=C(C=C1)I.[I-]

Technology Process of 2-(4-Iodophenoxy)-N,N,N-trimethylethan-1-aminium iodide

There total 7 articles about 2-(4-Iodophenoxy)-N,N,N-trimethylethan-1-aminium iodide 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%

: 93790-54-6
[2-(4-iodophenoxy)ethyl]dimethylamine

: 74-88-4
methyl iodide

: 93790-57-9
O-(4-iodophenyl)choline

Guidance literature:: In chloroform; for 0.5h; Ambient temperature;
DOI:10.1139/v84-344

Reference yield:

: 100-02-7,78813-13-5,89830-32-0
4-nitro-phenol

: 93790-57-9
O-(4-iodophenyl)choline

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) ethanol; 2.) water, toulene, reflux

2: 82 percent / 0.5 h / 0 °C

3: 1.) 50percent sulfuric acid, sodium nitrite; 2.) urea, sodium iodide-127, sodium sulfite / 1.) 0 deg C, 10 min, water; 2.) 10 min, 0 deg C, water; 3.) 10 min, r.t.; 4.) 6 min, 80 deg C

4: 95 percent / CHCl₃ / 0.5 h / Ambient temperature

With sodium [¹²⁷I]iodide; sulfuric acid; urea; sodium sulfite; sodium nitrite; In chloroform;
DOI:10.1139/v84-344

Reference yield:

: 540-38-5
p-Iodophenol

: 93790-57-9
O-(4-iodophenyl)choline

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) potassium hydroxide / 1.) ethanol, r.t.; 2.) toulene, reflux, overnight

2: 95 percent / CHCl₃ / 0.5 h / Ambient temperature

With potassium hydroxide; In chloroform;
DOI:10.1139/v84-344