4-[(4-nitrophenyl)carbamoyl]benzoic Acid

Base Information

Chemical Name:4-[(4-nitrophenyl)carbamoyl]benzoic Acid
CAS No.:72269-16-0
Molecular Formula:C14H10N2O5
Molecular Weight:286.244
Hs Code.:
DSSTox Substance ID:DTXSID00396056
Wikidata:Q82196533

Synonyms:4-[(4-nitrophenyl)carbamoyl]benzoic Acid;72269-16-0;Oprea1_531537;SCHEMBL7696438;DTXSID00396056

Suppliers and Price of 4-[(4-nitrophenyl)carbamoyl]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-[(4-nitrophenyl)carbamoyl]benzoic Acid

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:286.05897142
Heavy Atom Count:21
Complexity:404

Purity/Quality:: 95-738%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)NC2=CC=C(C=C2)[N+](=O)[O-])C(=O)O

Technology Process of 4-[(4-nitrophenyl)carbamoyl]benzoic Acid

There total 2 articles about 4-[(4-nitrophenyl)carbamoyl]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:

: 18708-46-8
terephthaloyl chloride

: 100-01-6,104810-17-5
4-nitro-aniline

: 72269-16-0
4-(carboxy)-N-(4-nitrophenyl)benzamide

Guidance literature:: With triethylamine; In tetrahydrofuran; dichloromethane; at 20 ℃; for 8h;
DOI:10.1039/d0ra03812a

Reference yield:

: 100-21-0
terephthalic acid

: 72269-16-0
4-(carboxy)-N-(4-nitrophenyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / dichloromethane / 2 h / 20 °C

2: triethylamine / dichloromethane; tetrahydrofuran / 8 h / 20 °C

With thionyl chloride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1039/d0ra03812a