2-[(4-Carboxyphenyl)carbamoyl]benzoic acid

Base Information

Chemical Name:2-[(4-Carboxyphenyl)carbamoyl]benzoic acid
CAS No.:19368-10-6
Molecular Formula:C15H11 N O5
Molecular Weight:285.256
Hs Code.:2924299090
DSSTox Substance ID:DTXSID10353615
Nikkaji Number:J1.508.752H
Wikidata:Q82131312
Mol file:19368-10-6.mol

Synonyms:2-[(4-carboxyphenyl)carbamoyl]benzoic acid;19368-10-6;2-[(4-CARBOXYANILINO)CARBONYL]BENZOIC ACID;2-[[(4-CARBOXYPHENYL)AMINO]CARBONYL]-BENZOIC ACID;2-{[(4-carboxyphenyl)amino]carbonyl}benzoic acid;2-[[(4-CARBOXYPHENYL)AMINO]CARBONyl]benZOIC ACID;CBDivE_003278;Oprea1_762349;SCHEMBL2058694;DTXSID10353615;AKOS002819475;SR-01000197330;SR-01000197330-1

Suppliers and Price of 2-[(4-Carboxyphenyl)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 3 raw suppliers

Chemical Property of 2-[(4-Carboxyphenyl)carbamoyl]benzoic acid

Chemical Property:

PSA：103.70000
LogP:2.40830
XLogP3:2.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:285.06372245
Heavy Atom Count:21
Complexity:414

Purity/Quality:: 99% ^*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)C(=O)O

Technology Process of 2-[(4-Carboxyphenyl)carbamoyl]benzoic acid

There total 7 articles about 2-[(4-Carboxyphenyl)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: 95.0%

: 85-44-9
phthalic anhydride

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

: 19368-10-6
2-[(4-carboxyphenyl)aminocarbonyl]benzoic acid

Guidance literature:: In chloroform; at 20 ℃; for 50h;
DOI:10.1039/b008399m

Reference yield:

: 2142-03-2
2-p-tolylisoindoline-1,3-dione

: 19368-10-6
2-[(4-carboxyphenyl)aminocarbonyl]benzoic acid

Guidance literature:: With potassium permanganate;

Reference yield:

: 106-49-0,12221-03-3
p-toluidine

: 19368-10-6
2-[(4-carboxyphenyl)aminocarbonyl]benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: bei der Destillation

2: potassium permanganate

With potassium permanganate;