N-Chloro-N-(2-chlorophenyl)acetamide

Base Information

Chemical Name:N-Chloro-N-(2-chlorophenyl)acetamide
CAS No.:29551-81-3
Molecular Formula:C8H7Cl2NO
Molecular Weight:204.056
Hs Code.:
DSSTox Substance ID:DTXSID90558186
Wikidata:Q82440384
Mol file:29551-81-3.mol

Synonyms:N-Chloro-N-(2-chlorophenyl)acetamide;29551-81-3;N,p-dichloroacetanilide;Acetanilide, N,2'-dichloro-;SCHEMBL3157322;DTXSID90558186

Suppliers and Price of N-Chloro-N-(2-chlorophenyl)acetamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-Chloro-N-(2-chlorophenyl)acetamide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:202.9904692
Heavy Atom Count:12
Complexity:174

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)N(C1=CC=CC=C1Cl)Cl

Technology Process of N-Chloro-N-(2-chlorophenyl)acetamide

There total 4 articles about N-Chloro-N-(2-chlorophenyl)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: 93.4%

: 533-17-5
N-(2-chlorophenyl)acetamide

: 29551-81-3
N-chloro-N-(2-chlorophenyl)acetamide

Guidance literature:: With trichloroisocyanuric acid; sodium hydrogencarbonate; In tert-butyl methyl ether; water; at 0 - 5 ℃; for 3h;

Reference yield:

: 95-51-2
o-chloroaniline

: 29551-81-3
N-chloro-N-(2-chlorophenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / water; tert-butyl methyl ether / 6 h / 0 - 20 °C

2: sodium hydrogencarbonate; trichloroisocyanuric acid / water; tert-butyl methyl ether / 3 h / 0 - 5 °C

With trichloroisocyanuric acid; sodium hydrogencarbonate; potassium hydroxide; In tert-butyl methyl ether; water;