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Details

Stereochemistry RACEMIC
Molecular Formula C16H12ClNO5
Molecular Weight 333.723
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENOXAPROP

SMILES

CC(OC1=CC=C(OC2=NC3=C(O2)C=C(Cl)C=C3)C=C1)C(O)=O

InChI

InChIKey=MPPOHAUSNPTFAJ-UHFFFAOYSA-N
InChI=1S/C16H12ClNO5/c1-9(15(19)20)21-11-3-5-12(6-4-11)22-16-18-13-7-2-10(17)8-14(13)23-16/h2-9H,1H3,(H,19,20)

HIDE SMILES / InChI

Molecular Formula C16H12ClNO5
Molecular Weight 333.723
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Structure of a tau class glutathione S-transferase from wheat active in herbicide detoxification.
2002 Jun 4
Characterisation of target-site resistance to ACCase-inhibiting herbicides in the weed Alopecurus myosuroides (black-grass).
2003 Feb
Factors associated with detection of bromoxynil in a sample of rural residents.
2003 Jan 24
Body mass index and bromoxynil exposure in a sample of rural residents during spring herbicide application.
2004 Sep 10
Influence of steric hindrance on enantioseparation of Dns-amino acids and pesticides on terguride based chiral selectors in capillary electrophoresis.
2005 May
Use of tert-butylbenzoylated tartardiamide chiral stationary phase for the enantiomeric resolution of acidic compounds by nano-liquid chromatography.
2006 Jul
Late watergrass (Echinochloa phyllopogon): mechanisms involved in the resistance to fenoxaprop-p-ethyl.
2007 May 16
Effect of herbicides on glutathione S-transferases in the earthworm, Eisenia fetida.
2008 Mar
Influence of toxicity and dissipation of racemic fenoxaprop and its R-enantiomer in Scenedesmus obliquus suspension by cyclodextrins.
2008 Mar-Apr
Cross-resistance patterns to ACCase-inhibiting herbicides conferred by mutant ACCase isoforms in Alopecurus myosuroides Huds. (black-grass), re-examined at the recommended herbicide field rate.
2008 Nov
Enantioselective environmental behavior of the chiral herbicide fenoxaprop-ethyl and its chiral metabolite fenoxaprop in soil.
2010 Dec 22
Prevalence of cross- or multiple resistance to the acetyl-coenzyme A carboxylase inhibitors fenoxaprop, clodinafop and pinoxaden in black-grass (Alopecurus myosuroides Huds.) in France.
2010 Feb
Cytosolic action of phytochelatin synthase.
2010 May
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:33:52 UTC 2023
Edited
by admin
on Sat Dec 16 09:33:52 UTC 2023
Record UNII
ZMB74WE9LB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENOXAPROP
Common Name English
2-(4-((6-CHLORO-2-BENZOXAZOLYL)OXY)PHENOXY)PROPANOIC ACID
Systematic Name English
PROPANOIC ACID, 2-(4-((6-CHLORO-2-BENZOXAZOLYL)OXY)PHENOXY)-, (±)-
Systematic Name English
HOE-53022
Code English
FENOXAPROP ACID
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 128701
Created by admin on Sat Dec 16 09:33:52 UTC 2023 , Edited by admin on Sat Dec 16 09:33:52 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID5058224
Created by admin on Sat Dec 16 09:33:52 UTC 2023 , Edited by admin on Sat Dec 16 09:33:52 UTC 2023
PRIMARY
ALANWOOD
fenoxaprop
Created by admin on Sat Dec 16 09:33:52 UTC 2023 , Edited by admin on Sat Dec 16 09:33:52 UTC 2023
PRIMARY
CAS
95617-09-7
Created by admin on Sat Dec 16 09:33:52 UTC 2023 , Edited by admin on Sat Dec 16 09:33:52 UTC 2023
PRIMARY
FDA UNII
ZMB74WE9LB
Created by admin on Sat Dec 16 09:33:52 UTC 2023 , Edited by admin on Sat Dec 16 09:33:52 UTC 2023
PRIMARY
PUBCHEM
86134
Created by admin on Sat Dec 16 09:33:52 UTC 2023 , Edited by admin on Sat Dec 16 09:33:52 UTC 2023
PRIMARY