N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine

Base Information

Chemical Name:N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine
CAS No.:134923-62-9
Molecular Formula:C10H16N2O
Molecular Weight:180.25
Hs Code.:2922199090
DSSTox Substance ID:DTXSID20604923
Wikidata:Q82503000
Mol file:134923-62-9.mol

Synonyms:N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine;134923-62-9;4-N-(2-methoxyethyl)-4-N-methylbenzene-1,4-diamine;SCHEMBL3039281;DTXSID20604923;UBMBWYARECKGQJ-UHFFFAOYSA-N;DB-063051;F75278;N-(2-Methoxyethyl)-N-methylbenzene-1,4-diamine;A1-41429;N~1~-(2-Methoxyethyl)-N~1~-methylbenzene-1,4-diamine

Suppliers and Price of N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine

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
N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine
10mg
$ 45.00

Crysdot
N1-(2-Methoxyethyl)-N1-methylbenzene-1,4-diamine 95+%
1g
$ 377.00

Total 14 raw suppliers

Chemical Property of N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine

Chemical Property:

Boiling Point:301.3±22.0 °C(Predicted)
PKA:6.74±0.50(Predicted)
PSA：38.49000
Density:1.066±0.06 g/cm3(Predicted)
LogP:1.93260
XLogP3:1.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:180.126263138
Heavy Atom Count:13
Complexity:133

Purity/Quality:

97% ^*data from raw suppliers

N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CCOC)C1=CC=C(C=C1)N

Technology Process of N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine

There total 3 articles about N1-(2-methoxyethyl)-N1-methylbenzene-1,4-diamine 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:

: 151951-34-7
N-(2-methoxyethyl)-N-methyl-4-nitroaniline

: 134923-62-9
N¹-(2-methoxyethyl)-N¹-methylbenzene-1,4-diamine

Guidance literature:: N-(2-methoxyethyl)-N-methyl-4-nitroaniline; With water; tin(ll) chloride; In ethanol; at 70 ℃;

With sodium hydroxide; In ethanol; water;

Reference yield:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 134923-62-9
N¹-(2-methoxyethyl)-N¹-methylbenzene-1,4-diamine

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 20 °C / Inert atmosphere

2: 5% Pd(II)/C(eggshell); hydrogen / tetrahydrofuran; methanol

With 5% Pd(II)/C(eggshell); hydrogen; triethylamine; In tetrahydrofuran; methanol;
DOI:10.1021/jm101580m

Reference yield:

: N-(2-methoxyethyl)-4-nitrobenzenamine

: 134923-62-9
N¹-(2-methoxyethyl)-N¹-methylbenzene-1,4-diamine

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydride / N,N-dimethyl-formamide / 0.17 h / 0 °C

2: hydrogen; palladium 10% on activated carbon / tetrahydrofuran / 40 °C

With palladium 10% on activated carbon; hydrogen; sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide;