Acetamide, 2,2,2-trifluoro-N-(4-methoxy-2-nitrophenyl)-

Base Information

Chemical Name:Acetamide, 2,2,2-trifluoro-N-(4-methoxy-2-nitrophenyl)-
CAS No.:128691-93-0
Molecular Formula:C9H7F3N2O4
Molecular Weight:264.161
Hs Code.:

Synonyms:2,2,2-Trifluoro-N-(4-methoxy-2-nitro-phenyl)-acetamide;N-<6-Nitro-4-methoxy-phenyl>-trifluoracetamid;4-methoxy-2-nitrotrifluoroanilide;

Suppliers and Price of Acetamide, 2,2,2-trifluoro-N-(4-methoxy-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
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price

Aronis compounds
2,2,2-trifluoro-N-(4-methoxy-2-nitrophenyl)acetamide
20mg
$ 30.00

Total 1 raw suppliers

Chemical Property of Acetamide, 2,2,2-trifluoro-N-(4-methoxy-2-nitrophenyl)-

Chemical Property:

PSA：84.15000
LogP:2.70040

Purity/Quality:: 2,2,2-trifluoro-N-(4-methoxy-2-nitrophenyl)acetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Acetamide, 2,2,2-trifluoro-N-(4-methoxy-2-nitrophenyl)-

There total 4 articles about Acetamide, 2,2,2-trifluoro-N-(4-methoxy-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: 82.0%

: 407-25-0
trifluoroacetic anhydride

: 96-96-8
4-methoxy-2-nitroaniline

: 128691-93-0
4-methoxy-2-nitrotrifluoroacetanilide

Guidance literature:: In acetonitrile; for 3h; Heating / reflux;

Reference yield: 63.0%

: 332-34-3
2,2,2-trifluoro-N-(4-methoxy-phenyl)-acetamide

: 128691-93-0
4-methoxy-2-nitrotrifluoroacetanilide

Guidance literature:: With sulfuric acid; nitric acid; In acetic acid; for 0.5h; Ambient temperature;

Reference yield:

: 104-94-9
4-methoxy-aniline

: 128691-93-0
4-methoxy-2-nitrotrifluoroacetanilide

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether / 1 h / 0 °C

2: 63 percent / conc. sulfuric acid, conc. nitric acid / acetic acid / 0.5 h / Ambient temperature

With sulfuric acid; nitric acid; In diethyl ether; acetic acid;