N-(3-Chlorophenyl)-N-hydroxybenzamide

Base Information

Chemical Name:N-(3-Chlorophenyl)-N-hydroxybenzamide
CAS No.:67055-91-8
Molecular Formula:C13H10ClNO2
Molecular Weight:247.681
Hs Code.:
DSSTox Substance ID:DTXSID00530099
Nikkaji Number:J2.663.098C
Wikidata:Q82401006

Synonyms:N-(3-Chlorophenyl)-N-hydroxybenzamide;67055-91-8;DTXSID00530099

Suppliers and Price of N-(3-Chlorophenyl)-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 1 raw suppliers

Chemical Property of N-(3-Chlorophenyl)-N-hydroxybenzamide

Chemical Property:

Vapor Pressure:0mmHg at 25°C
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:247.0400063
Heavy Atom Count:17
Complexity:266

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=CC(=CC=C2)Cl)O

Technology Process of N-(3-Chlorophenyl)-N-hydroxybenzamide

There total 1 articles about N-(3-Chlorophenyl)-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:

: 10468-17-4
N-(3-chlorophenyl)hydroxylamine

: 98-88-4
benzoyl chloride

: 67055-91-8
N-(m-Chlorophenyl)benzohydroxamic acid

Guidance literature:: With sodium hydrogencarbonate; In water; benzene; at 0 - 5 ℃; for 2.5h; Yield given;
DOI:10.1055/s-1984-31027

Reference yield: 53.0%

: 67055-91-8
N-(m-Chlorophenyl)benzohydroxamic acid

: 10286-77-8
N-(2,3-dichlorophenyl)benzamide

: 6626-75-1
N-(2,5-dichlorophenyl)benzamide

Guidance literature:: With thionyl chloride; In diethyl ether; for 1h; T < 5 deg C;

Reference yield:

: 67055-91-8
N-(m-Chlorophenyl)benzohydroxamic acid

: 608-27-5
2,3-dichloroaniline

Guidance literature:: Multi-step reaction with 2 steps

1: 53 percent / SOCl₂ / diethyl ether / 1 h / T < 5 deg C

2: 89 percent / 70percent H₂SO₄ / 3 h / Heating

With thionyl chloride; sulfuric acid; In diethyl ether;