N-(2,5-Dichlorophenyl)-N-hydroxybenzamide

Base Information

Chemical Name:N-(2,5-Dichlorophenyl)-N-hydroxybenzamide
CAS No.:88963-37-5
Molecular Formula:C13H9Cl2NO2
Molecular Weight:282.126
Hs Code.:
DSSTox Substance ID:DTXSID90525373
Wikidata:Q82392929

Synonyms:N-(2,5-Dichlorophenyl)-N-hydroxybenzamide;88963-37-5;DTXSID90525373

Suppliers and Price of N-(2,5-Dichlorophenyl)-N-hydroxybenzamide

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-Dichlorophenyl)-N-hydroxybenzamide

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:281.0010339
Heavy Atom Count:18
Complexity:295

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)N(C2=C(C=CC(=C2)Cl)Cl)O

Technology Process of N-(2,5-Dichlorophenyl)-N-hydroxybenzamide

There total 2 articles about N-(2,5-Dichlorophenyl)-N-hydroxybenzamide 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:

: 89-61-2
2,5-dichloronitrobenzene

: 88963-37-5
N-(2,5-Dichlorophenyl)benzohydroxamic acid

Guidance literature:: Multi-step reaction with 2 steps

1: Zinc dust, NH₄Cl (or NH₄Br)

2: NaHCO₃ / diethyl ether; H₂O / 1 h / T < 5 deg C; or in benzene

With sodium hydrogencarbonate; ammonium chloride; zinc; In diethyl ether; water;