Acetamide, N-[4-(4-chlorobutoxy)-2-nitrophenyl]-

Base Information

Chemical Name:Acetamide, N-[4-(4-chlorobutoxy)-2-nitrophenyl]-
CAS No.:152538-17-5
Molecular Formula:C12H15ClN2O4
Molecular Weight:286.715
Hs Code.:
DSSTox Substance ID:DTXSID20435037
Wikidata:Q82249712
Mol file:152538-17-5.mol

Synonyms:152538-17-5;Acetamide, N-[4-(4-chlorobutoxy)-2-nitrophenyl]-;DTXSID20435037

Suppliers and Price of Acetamide, N-[4-(4-chlorobutoxy)-2-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-[4-(4-chlorobutoxy)-2-nitrophenyl]-

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:286.0720347
Heavy Atom Count:19
Complexity:309

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=C(C=C(C=C1)OCCCCCl)[N+](=O)[O-]

Technology Process of Acetamide, N-[4-(4-chlorobutoxy)-2-nitrophenyl]-

There total 3 articles about Acetamide, N-[4-(4-chlorobutoxy)-2-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: 90.0%

: 6940-78-9
4-chlorobutyl bromide

: 7403-75-0
N-(4-hydroxy-2-nitrophenyl)-acetamide

: 152538-17-5
N-[4-(4-chlorobutoxy)-2-nitrophenyl]acetamide

Guidance literature:: With sodium carbonate; potassium iodide; In N,N-dimethyl-formamide; at 50 ℃; for 24h;
DOI:10.1016/j.bmc.2005.09.063

Reference yield: 60.0%

: 152538-15-3
4-(4-chlorobutoxy)acetanilide

: 152538-17-5
N-[4-(4-chlorobutoxy)-2-nitrophenyl]acetamide

Guidance literature:: With nitric acid; acetic acid; for 24h; Ambient temperature;
DOI:10.1002/jhet.5570300205

Reference yield:

: 103-90-2,8055-08-1
4-acetaminophenol

: 152538-17-5
N-[4-(4-chlorobutoxy)-2-nitrophenyl]acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / K₂CO₃ / ethanol / Heating

2: 60 percent / 18percent aq. HNO₃, glacial AcOH / 24 h / Ambient temperature

With nitric acid; potassium carbonate; acetic acid; In ethanol;
DOI:10.1002/jhet.5570300205