4-(2-Chlorobenzamido)benzoic acid

Base Information

Chemical Name:4-(2-Chlorobenzamido)benzoic acid
CAS No.:70204-54-5
Molecular Formula:C14H10ClNO3
Molecular Weight:275.691
Hs Code.:
DSSTox Substance ID:DTXSID90360645
Wikidata:Q82142492

Synonyms:4-(2-chlorobenzamido)benzoic acid;70204-54-5;Benzoic acid, 4-[(2-chlorobenzoyl)amino]-;Cambridge id 5260276;Oprea1_343551;SCHEMBL4254327;DTXSID90360645;QBAQNDNVEWMANU-UHFFFAOYSA-N;AKOS000105115

Suppliers and Price of 4-(2-Chlorobenzamido)benzoic acid

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 4-(2-Chlorobenzamido)benzoic acid

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:275.0349209
Heavy Atom Count:19
Complexity:340

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)NC2=CC=C(C=C2)C(=O)O)Cl

Technology Process of 4-(2-Chlorobenzamido)benzoic acid

There total 5 articles about 4-(2-Chlorobenzamido)benzoic acid 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: 54.2%

: 609-65-4
o-chlorobenzoyl chloride

: 150-13-0,159246-81-8,8014-65-1
4-amino-benzoic acid

: 70204-54-5
4-(2-chlorobenzamido)benzoic acid

Guidance literature:: o-chlorobenzoyl chloride; 4-amino-benzoic acid; With triethylamine; In acetonitrile; at 20 ℃; for 4h; Inert atmosphere;

With sodium hydroxide; In diethyl ether; water;

With hydrogenchloride; In water; pH=2;

Reference yield:

: 75121-10-7
2-chloro-4'-ethoxycarbonylbenzanilide

: 70204-54-5
4-(2-chlorobenzamido)benzoic acid

Guidance literature:: With methanol; sodium hydroxide; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1016/j.bmcl.2011.11.101

Reference yield:

: 94-09-7
p-aminoethylbenzoate

: 70204-54-5
4-(2-chlorobenzamido)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 3 h / 20 °C / Inert atmosphere

2: methanol; sodium hydroxide / tetrahydrofuran / 2 h / 20 °C

With methanol; dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2011.11.101