2-[(4-Aminobenzoyl)amino]benzoic acid

Base Information

Chemical Name:2-[(4-Aminobenzoyl)amino]benzoic acid
CAS No.:60498-39-7
Molecular Formula:C14H12N2O3
Molecular Weight:256.261
Hs Code.:
DSSTox Substance ID:DTXSID90354620
Wikidata:Q82132866
ChEMBL ID:CHEMBL1505441

Synonyms:2-[(4-aminobenzoyl)amino]benzoic acid;60498-39-7;MLS000530201;STK259710;SMR000135178;2-{[(4-aminophenyl)carbonyl]amino}benzoic acid;CBMicro_013206;Oprea1_258208;cid_777056;SCHEMBL1307695;CHEMBL1505441;BDBM68763;DTXSID90354620;HMS2372G10;SMSF0004152;AKOS001625043;CB03149;2-(4-AMINOBENZAMIDO)BENZOIC ACID;BIM-0013218.P001;CS-0358677;EU-0037925;2-[(4-aminophenyl)carbonylamino]benzoic acid;2-[[(4-aminophenyl)-oxomethyl]amino]benzoic acid;SR-01000430997;SR-01000430997-1

Suppliers and Price of 2-[(4-Aminobenzoyl)amino]benzoic acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-[(4-Aminobenzoyl)amino]benzoic acid

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:256.08479225
Heavy Atom Count:19
Complexity:338

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 2-[(4-Aminobenzoyl)amino]benzoic acid

There total 7 articles about 2-[(4-Aminobenzoyl)amino]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: 96.0%

: 180133-07-7
methyl 2-(4-aminobenzamido)benzoate

: 60498-39-7
2-(4-aminobenzamido)benzoic acid

Guidance literature:: With water; sodium hydroxide; In methanol; dichloromethane; Reflux;
DOI:10.1007/s00044-012-0269-6

Reference yield:

: 6345-04-6
N-(4-nitrobenzoyl)anthranilic acid

: 60498-39-7
2-(4-aminobenzamido)benzoic acid

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 2h;
DOI:10.3390/molecules24152780

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 60498-39-7
2-(4-aminobenzamido)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / 20 °C

2: palladium 10% on activated carbon; hydrogen / methanol / 2 h / 20 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; In methanol;
DOI:10.3390/molecules24152780