N-hydroxy-N-[4-(2,4,6-trichlorophenoxy)phenyl]acetamide

Base Information

Chemical Name:N-hydroxy-N-[4-(2,4,6-trichlorophenoxy)phenyl]acetamide
CAS No.:98911-09-2
Molecular Formula:C14H10Cl3NO3
Molecular Weight:346.5931
Hs Code.:

Synonyms:N-hydroxy-4-(2,4-6-trichlorophenoxy)acetanilide;2,4,6-Trichloro-4'-hydroxyacetylaminobiphenyl ether;N-Hydroxy-N-(4-(2,4,6-trichlorophenoxy)phenyl)acetamide;

Suppliers and Price of N-hydroxy-N-[4-(2,4,6-trichlorophenoxy)phenyl]acetamide

Supply Marketing:

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

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Chemical Property of N-hydroxy-N-[4-(2,4,6-trichlorophenoxy)phenyl]acetamide

Chemical Property:

Vapor Pressure:1.09E-08mmHg at 25°C
Boiling Point:444.6°Cat760mmHg
PKA:8.57±0.50(Predicted)
Flash Point:222.7°C
PSA：49.77000
Density:1.516g/cm³
LogP:5.18120

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-hydroxy-N-[4-(2,4,6-trichlorophenoxy)phenyl]acetamide

There total 2 articles about N-hydroxy-N-[4-(2,4,6-trichlorophenoxy)phenyl]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:

: 98911-25-2
N-acetyl-4-(2,4,6-trichlorophenoxy)anilino β-D-glucopyranoside

: 98911-09-2
2,4,6-Trichloro-4'-hydroxyacetylaminobiphenyl ether

Guidance literature:: With sodium acetate buffer; β-glucosidase; at 37 ℃; for 0.5h;

Reference yield:

: 1836-77-7
p-nitrophenyl 2,4,6-trichlorophenyl ether

: 75-36-5
acetyl chloride

: 98911-09-2
2,4,6-Trichloro-4'-hydroxyacetylaminobiphenyl ether

Guidance literature:: With ammonium chloride; sodium hydrogencarbonate; zinc; Yield given. Multistep reaction; 1.) dioxane, 15 min 2.) ether, water, 1.5 h;