Acetamide, N-(5-ethoxy-2-methyl-4-nitrophenyl)-

Base Information

Chemical Name:Acetamide, N-(5-ethoxy-2-methyl-4-nitrophenyl)-
CAS No.:361162-91-6
Molecular Formula:C11H14N2O4
Molecular Weight:238.243
Hs Code.:
DSSTox Substance ID:DTXSID50451785
Wikidata:Q82272005
Mol file:361162-91-6.mol

Synonyms:Acetamide, N-(5-ethoxy-2-methyl-4-nitrophenyl)-;361162-91-6;SCHEMBL3266352;DTXSID50451785

Suppliers and Price of Acetamide, N-(5-ethoxy-2-methyl-4-nitrophenyl)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Acetamide, N-(5-ethoxy-2-methyl-4-nitrophenyl)-

Chemical Property:

PSA：87.64000
LogP:3.43300
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:238.09535693
Heavy Atom Count:17
Complexity:290

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC1=C(C=C(C(=C1)NC(=O)C)C)[N+](=O)[O-]

Technology Process of Acetamide, N-(5-ethoxy-2-methyl-4-nitrophenyl)-

There total 4 articles about Acetamide, N-(5-ethoxy-2-methyl-4-nitrophenyl)- 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: 53.0%

: 361162-90-5
5-methoxy-2-methyl-4-nitroacetanilide

: 75-03-6
ethyl iodide

: 361162-91-6
5-ethoxy-2-methyl-4-nitroacetanilide

Guidance literature:: With magnesium sulfate; potassium carbonate; lithium chloride; In chloroform; N,N-dimethyl-formamide;

Reference yield:

: 106579-00-4
5-methoxy-2-methyl-4-nitroaniline

: 361162-91-6
5-ethoxy-2-methyl-4-nitroacetanilide

Guidance literature:: Multi-step reaction with 3 steps

1: 65 percent / AcOH / 0.5 h / Heating

2: LiCl / dimethylformamide / 12 h / Heating

3: K₂CO₃ / dimethylformamide / 5 h / Heating

With potassium carbonate; acetic acid; lithium chloride; In N,N-dimethyl-formamide;
DOI:10.1021/jm020241c

Reference yield:

: 361162-90-5
5-methoxy-2-methyl-4-nitroacetanilide

: 361162-91-6
5-ethoxy-2-methyl-4-nitroacetanilide

Guidance literature:: Multi-step reaction with 2 steps

1: LiCl / dimethylformamide / 12 h / Heating

2: K₂CO₃ / dimethylformamide / 5 h / Heating

With potassium carbonate; lithium chloride; In N,N-dimethyl-formamide;
DOI:10.1021/jm020241c