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Details

Stereochemistry ACHIRAL
Molecular Formula C8H7NO3
Molecular Weight 165.1461
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXANILIC ACID

SMILES

OC(=O)C(=O)NC1=CC=CC=C1

InChI

InChIKey=PQJZHMCWDKOPQG-UHFFFAOYSA-N
InChI=1S/C8H7NO3/c10-7(8(11)12)9-6-4-2-1-3-5-6/h1-5H,(H,9,10)(H,11,12)

HIDE SMILES / InChI

Molecular Formula C8H7NO3
Molecular Weight 165.1461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Simultaneous screening of herbicide degradation byproducts in water treatment plants using high performance liquid chromatography-tandem mass spectrometry.
2010-04-28
Direct aqueous injection LC-ESI/MS/MS analysis of water for 11 chloro- and thiomethyltriazines and metolachlor and its ethanesulfonic and oxanilic acid degradates.
2008-04-23
Chemical hybridizing agents for chickpea (Cicer arietinum L.): leads from QSAR analysis of ethyl oxanilates and pyridones.
2006-03-08
Development of EPA method 535 for the determination of chloroacetanilide and other acetamide herbicide degradates in drinking water by solid-phase extraction and liquid chromatography/tandem mass spectrometry.
2006-03-04
Enantiomeric separation of metolachlor and its metabolites using LC-MS and CZE.
2006-03
Are neutral chloroacetamide herbicide degradates of potential environmental concern? Analysis and occurrence in the upper Chesapeake Bay.
2005-09-01
Degradation of metolachlor in bare and vegetated soils and in simulated water-sediment systems.
2004-11
Infiltration of acetochlor and two of its metabolites in two contrasting soils.
2004-02-18
Novel chromatographic separation and carbon solid-phase extraction of acetanilide herbicide degradation products.
2002-12-13
Analytical method for the determination of metolachlor, acetochlor, alachlor, dimethenamid, and their corresponding ethanesulfonic and oxanillic acid degradates in water using SPE and LC/ESI-MS/MS.
2002-08-01
Determination of oxanilic and sulfonic acid metabolites of acetochlor in soils by liquid chromatography-electrospray ionisation mass spectrometry.
2002-05-24
Structure-metabolism relationships of substituted anilines: prediction of N-acetylation and N-oxanilic acid formation using computational chemistry.
2002-04
Analysis and detection of the herbicides dimethenamid and flufenacet and their sulfonic and oxanilic acid degradates in natural water.
2002-02-27
Anaerobic degradation of atrazine and metolachlor and metabolite formation in wetland soil and water microcosms.
2001-07-31
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:24:33 GMT 2025
Edited
by admin
on Mon Mar 31 19:24:33 GMT 2025
Record UNII
136B46378D
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-47546
Preferred Name English
OXANILIC ACID
Common Name English
N-PHENYLOXAMIC ACID
Systematic Name English
2-OXO-2-(PHENYLAMINO)ACETIC ACID
Systematic Name English
ACETIC ACID, OXO(PHENYLAMINO)-
Systematic Name English
OXAMIC ACID, PHENYL-
Systematic Name English
ACETIC ACID, 2-OXO-2-(PHENYLAMINO)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID4060105
Created by admin on Mon Mar 31 19:24:33 GMT 2025 , Edited by admin on Mon Mar 31 19:24:33 GMT 2025
PRIMARY
CAS
500-72-1
Created by admin on Mon Mar 31 19:24:33 GMT 2025 , Edited by admin on Mon Mar 31 19:24:33 GMT 2025
PRIMARY
PUBCHEM
10378
Created by admin on Mon Mar 31 19:24:33 GMT 2025 , Edited by admin on Mon Mar 31 19:24:33 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-910-9
Created by admin on Mon Mar 31 19:24:33 GMT 2025 , Edited by admin on Mon Mar 31 19:24:33 GMT 2025
PRIMARY
FDA UNII
136B46378D
Created by admin on Mon Mar 31 19:24:33 GMT 2025 , Edited by admin on Mon Mar 31 19:24:33 GMT 2025
PRIMARY
NSC
47546
Created by admin on Mon Mar 31 19:24:33 GMT 2025 , Edited by admin on Mon Mar 31 19:24:33 GMT 2025
PRIMARY