Benzenamine, N-(2-methoxyethyl)-2,6-dimethyl-

Base Information

Chemical Name:Benzenamine, N-(2-methoxyethyl)-2,6-dimethyl-
CAS No.:50563-55-8
Molecular Formula:C11H17 N O
Molecular Weight:179.262
Hs Code.:2922199090
European Community (EC) Number:256-626-1
DSSTox Substance ID:DTXSID2068555
Nikkaji Number:J261.539H
Wikidata:Q81995309
Mol file:50563-55-8.mol

Synonyms:50563-55-8;N-(2-methoxyethyl)-2,6-dimethylaniline;Benzenamine, N-(2-methoxyethyl)-2,6-dimethyl-;EINECS 256-626-1;N-(2-Methoxyethyl)-2,6-xylidine;2,6-Dimethyl-N-(2'-methoxyethyl)aniline;2,6-dimethyl-N-(2'-methoxyethyl)-aniline;DTXSID2068555;SCHEMBL11310203;AKOS011616318;N-(2-Methoxyethyl)-2,6-dimethylbenzenamine

Suppliers and Price of Benzenamine, N-(2-methoxyethyl)-2,6-dimethyl-

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

TRC
N-(2-Methoxyethyl)-2,6-xylidine
1g
$ 1165.00

TRC
N-(2-Methoxyethyl)-2,6-xylidine
100mg
$ 155.00

Total 5 raw suppliers

Chemical Property of Benzenamine, N-(2-methoxyethyl)-2,6-dimethyl-

Chemical Property:

Vapor Pressure:0.00194mmHg at 25°C
Boiling Point:291.5°C at 760 mmHg
PKA:4.12±0.50(Predicted)
Flash Point:117.2°C
PSA：21.26000
Density:0.991g/cm³
LogP:2.43470
Solubility.:DMSO; Toluene; Chloroform;
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:179.131014166
Heavy Atom Count:13
Complexity:128

Purity/Quality:

99% ^*data from raw suppliers

N-(2-Methoxyethyl)-2,6-xylidine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=CC=C1)C)NCCOC
Uses N-(2-Methoxyethyl)-2,6-xylidine is an intermediate used in the synthesis of Dimethachlor Ethane Sulfonic Acid Sodium Salt (D460283), which is a pesticide metabolite pollutant found in groundwater, surface water, and wastewater.

Technology Process of Benzenamine, N-(2-methoxyethyl)-2,6-dimethyl-

There total 9 articles about Benzenamine, N-(2-methoxyethyl)-2,6-dimethyl- 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:

: 40790-56-5
2,6-dimethyl-2-cyclohexen-1-one

: 109-85-3
2-methoxyethylamine

: 50563-55-8
2,6-dimethyl-N-(2'-methoxyethyl)-aniline

Guidance literature:: palladium on charcoal; In toluene;

Reference yield:

: 73621-38-2
N-(2-methoxyethyl)-2,6-dimethylcyclohex-2-en-1-one-imine

: 187737-37-7,13987-01-4,15220-87-8,9003-07-0,676-63-1,25085-53-4
propene

: 50563-55-8
2,6-dimethyl-N-(2'-methoxyethyl)-aniline

Guidance literature:: palladium on charcoal; In 1,4-dioxane;

Reference yield:

: 87-62-7
2,6-dimethylaniline

: 50563-55-8
2,6-dimethyl-N-(2'-methoxyethyl)-aniline

Guidance literature:: Multi-step reaction with 3 steps

1: 96.5 percent / 10percent aq.NaOH / toluene / 1.17 h / 25 °C

2: 95.7 percent / 25percent methanolic NaOCH₃ / methanol / 5 h / Ambient temperature

3: 2.) 6M HCl / 1.) methanol, 83 deg C, 6 h, 2.) 30 min, reflux

With hydrogenchloride; sodium hydroxide; sodium methylate; In methanol; toluene;
DOI:10.1016/S0040-4039(00)80688-7