N-(2,5-dibromo-4-nitrophenyl)acetamide

Base Information

Chemical Name:N-(2,5-dibromo-4-nitrophenyl)acetamide
CAS No.:25462-67-3
Molecular Formula:C8H6Br2N2O3
Molecular Weight:337.955
Hs Code.:
DSSTox Substance ID:DTXSID40462461
Nikkaji Number:J1.528.954F
Wikidata:Q82287003

Synonyms:N-(2,5-dibromo-4-nitrophenyl)acetamide;25462-67-3;SCHEMBL5069542;2,5-dibromo-4-nitroacetanilide;DTXSID40462461;AB9033;MFCD14582987;AS-44939

Suppliers and Price of N-(2,5-dibromo-4-nitrophenyl)acetamide

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 2 raw suppliers

Chemical Property of N-(2,5-dibromo-4-nitrophenyl)acetamide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:337.87247
Heavy Atom Count:15
Complexity:269

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC(=C(C=C1Br)[N+](=O)[O-])Br

Technology Process of N-(2,5-dibromo-4-nitrophenyl)acetamide

There total 5 articles about N-(2,5-dibromo-4-nitrophenyl)acetamide 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: 97.71%

: 25462-66-2
N-(2,5-dibromophenyl)acetamide

: 25462-67-3
N-(2,5-dibromo-4-nitrophenyl)acetamide

Guidance literature:: With sulfuric acid; nitric acid; at 30 ℃; for 0.666667h;

Reference yield:

: 3638-73-1
2,5-dibromoaniline

: 25462-67-3
N-(2,5-dibromo-4-nitrophenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 27 g / Et₃N / 1 h / 35 °C

2: 63 percent / HNO₃; H₂SO₄ / -20 - 20 °C

With sulfuric acid; nitric acid; triethylamine;
DOI:10.1016/j.tet.2003.10.089

Reference yield:

: 106-37-6
1.4-dibromobenzene

: 25462-67-3
N-(2,5-dibromo-4-nitrophenyl)acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / sulfuric acid; nitric acid / CH₂Cl₂ / 1 h

2: SnCl₂*2H₂O / ethanol; tetrahydrofuran / 0.5 h

3: 27 g / Et₃N / 1 h / 35 °C

4: 63 percent / HNO₃; H₂SO₄ / -20 - 20 °C

With sulfuric acid; nitric acid; triethylamine; tin(ll) chloride; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1016/j.tet.2003.10.089