Acetamide, 2,2,2-trichloro-N-(2-nitrophenyl)-

Base Information

Chemical Name:Acetamide, 2,2,2-trichloro-N-(2-nitrophenyl)-
CAS No.:23326-83-2
Molecular Formula:C₈H₅Cl₃N₂O₃
Molecular Weight:283.498
Hs Code.:2924299090
DSSTox Substance ID:DTXSID90945996
Nikkaji Number:J130.467D
Wikidata:Q82923449
Mol file:23326-83-2.mol

Synonyms:Acetamide, 2,2,2-trichloro-N-(2-nitrophenyl)-;23326-83-2;2,2,2-Trichloro-N-(2-nitrophenyl)acetamide;DTXSID90945996;NCZQSPCRTZSEAC-UHFFFAOYSA-N;AKOS003867891;2,2,2-Trichloro-N-(2-nitrophenyl)acetamide #;2,2,2-Trichloro-N-(2-nitrophenyl)ethanimidic acid

Suppliers and Price of Acetamide, 2,2,2-trichloro-N-(2-nitrophenyl)-

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 3 raw suppliers

Chemical Property of Acetamide, 2,2,2-trichloro-N-(2-nitrophenyl)-

Chemical Property:

Vapor Pressure:1.29E-06mmHg at 25°C
Boiling Point:400.3°C at 760 mmHg
Flash Point:195.9°C
PSA：78.41000
Density:1.681g/cm³
LogP:4.07620
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:281.936575
Heavy Atom Count:16
Complexity:287

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Acetamide, 2,2,2-trichloro-N-(2-nitrophenyl)-

There total 7 articles about Acetamide, 2,2,2-trichloro-N-(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:

: 62-53-3
aniline

: 23326-83-2
N-(2-nitrophenyl)-2,2,2,-trichloroacetamide

Guidance literature:: Multi-step reaction with 2 steps

2: NO₂, O₃, O₂ / CHCl₃ / 3.5 h / 0 °C

With oxygen; Nitrogen dioxide; ozone; In chloroform;

Reference yield:

: 2563-97-5
2,2,2-trichloro-N-phenylacetamide

: 23326-83-2
N-(2-nitrophenyl)-2,2,2,-trichloroacetamide

: 4306-32-5
N-(4-nitrophenyl)-2,2,2,-trichloroacetamide

Guidance literature:: With nitric acid;

Reference yield:

: 62-53-3
aniline

: 23326-83-2
N-(2-nitrophenyl)-2,2,2,-trichloroacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: benzene

2: HNO₃+H₂SO₄ / in der Kaelte

With sulfuric acid; nitric acid; benzene;