4-(Oxaloamino)benzoic acid

Base Information

Chemical Name:4-(Oxaloamino)benzoic acid
CAS No.:14121-56-3
Molecular Formula:C9H7NO5
Molecular Weight:209.158
Hs Code.:
DSSTox Substance ID:DTXSID801284423
Nikkaji Number:J494.466F
Wikidata:Q27114009
Metabolomics Workbench ID:54275
ChEMBL ID:CHEMBL540439

Synonyms:4-(oxaloamino)benzoic acid;4-[(carboxycarbonyl)amino]benzoic acid;CHEBI:30875;14121-56-3;CHEMBL540439;DTXSID801284423;Benzoic acid, 4-[(carboxycarbonyl)amino]-;4-[(2-Hydroxy-1,2-dioxoethyl)amino]benzoic acid;Q27114009

Suppliers and Price of 4-(Oxaloamino)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 4-(Oxaloamino)benzoic acid

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:209.03242232
Heavy Atom Count:15
Complexity:280

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)O)NC(=O)C(=O)O

Technology Process of 4-(Oxaloamino)benzoic acid

There total 6 articles about 4-(Oxaloamino)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: 23.0%

: 141635-22-5
ethyl 4-(2-methoxy-2-oxoacetamido)benzoate

: 14121-56-3
4-(carboxyformamido)benzoic acid

Guidance literature:: With sodium hydroxide; Amberlite JR-120(H); for 2h; Ambient temperature;
DOI:10.1021/jm00092a016

Reference yield:

: 4-(2-methoxy-2-oxoacetamido)benzoic acid

: 14121-56-3
4-(carboxyformamido)benzoic acid

Guidance literature:: With sodium hydroxide; In methanol; for 0.166667h;
DOI:10.3390/molecules26165009

Reference yield:

: 94-09-7
p-aminoethylbenzoate

: 14121-56-3
4-(carboxyformamido)benzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / toluene / 4 h / Heating

2: 23 percent / 1.) aq. sodium hydroxide, 2.) Amberlite JR-120(H) / 2 h / Ambient temperature

With sodium hydroxide; Amberlite JR-120(H); In toluene;
DOI:10.1021/jm00092a016