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Details

Stereochemistry ACHIRAL
Molecular Formula C19H15FN2O4
Molecular Weight 354.3318
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUMIOXAZIN

SMILES

FC1=C(C=C2N(CC#C)C(=O)COC2=C1)N3C(=O)C4=C(CCCC4)C3=O

InChI

InChIKey=FOUWCSDKDDHKQP-UHFFFAOYSA-N
InChI=1S/C19H15FN2O4/c1-2-7-21-15-9-14(13(20)8-16(15)26-10-17(21)23)22-18(24)11-5-3-4-6-12(11)19(22)25/h1,8-9H,3-7,10H2

HIDE SMILES / InChI

Molecular Formula C19H15FN2O4
Molecular Weight 354.3318
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Dermal developmental toxicity of N-phenylimide herbicides in rats.
2014-04
rac-6-Hy-droxy-4-(4-nitro-phen-yl)-5-(2-thienyl-carbon-yl)-6-(trifluoro-meth-yl)-3,4,5,6-tetra-hydro-pyrimidin-2(1H)-one monohydrate.
2010-10-23
6-Hy-droxy-4-(pyridin-3-yl)-5-(2-thienyl-carbon-yl)-6-trifluoro-meth-yl-3,4,5,6-tetra-hydro-pyrimidin-2(1H)-one.
2010-10-20
rac-Ethyl 4-hy-droxy-6-(2-hy-droxy-phen-yl)-2-oxo-4-(trifluoro-methyl)per-hydro-pyrimidine-5-carboxyl-ate.
2010-06-16
Ethyl 6-[4-(dimethyl-amino)phen-yl]-4-hydr-oxy-2-oxo-4-(trifluoro-methyl)-hexa-hydro-pyrimidine-5-carboxyl-ate.
2010-04-14
Synthesis and herbicidal activity of isoindoline-1,3-dione substituted benzoxazinone derivatives containing a carboxylic ester group.
2009-10-28
5-Benzoyl-4-hydr-oxy-6-(4-nitro-phen-yl)-4-trifluoro-meth-yl-3,4,5,6-tetrahydro-pyrimidin-2(1H)-one monohydrate.
2008-12-10
Ethyl 4-(4-nitro-phen-yl)-2-(trifluoro-meth-yl)pyrimido[1,2-a]benzimidazole-3-carboxyl-ate.
2008-11-29
2-Amino-1H-benzoimidazol-3-ium 4,4,4-trifluoro-1,3-dioxo-1-phenyl-butan-2-ide.
2008-11-26
The herbicide flumioxazin stimulates pathogenesis-related gene expression and enzyme activities in Vitis vinifera.
2008-11
3-Ethyl 5-methyl 2-hydr-oxy-6-methyl-4-(4-nitro-phen-yl)-2-trifluoro-methyl-1,2,3,4-tetra-hydro-pyridine-3,5-dicarboxyl-ate.
2008-08-09
[Determination of flumioxazin residue in foods using gas chromatography-mass spectrometry].
2008-05
Dissipation and movement of flumioxazin in soil at four field sites in Chile.
2008-05
Chemical cotton stalk destruction for maintenance of host-free periods for the control of overwintering boll weevil in tropical and subtropical climates.
2007-04
Effect of the herbicide flumioxazin on photosynthetic performance of grapevine (Vitis vinifera L.).
2007-04
Evaluation of six pesticides leaching indexes using field data of herbicide application in Casablanca Valley, Chile.
2007
Proteomic analysis of grapevine (Vitis vinifera L.) tissues subjected to herbicide stress.
2005-11
Synthesis and herbicidal activity of 2-(7-fluoro-3-oxo- 3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)isoindoline-1,3-diones.
2005-10-05
Protoporphyrinogen oxidase inhibitor herbicide effects on pythium root rot of sugarcane, pythium species, and the soil microbial community.
2005-03
Sorption and desorption of flumioxazin to soil, clay minerals and ion-exchange resin.
2005-01
Hydrolysis and photolysis of flumioxazin in aqueous buffer solutions.
2004-09
Comparison of different physiological parameter responses in Lemna minor and Scenedesmus obliquus exposed to herbicide flumioxazin.
2004-09
Gas chromatographic/mass spectrometric determination of flumioxazin extracted from soil and water.
2004-04-16
Stress reactions in Vitis vinifera L. following soil application of the herbicide flumioxazin.
2003-10
Stress effects of flumioxazin herbicide on grapevine ( Vitis vinifera L.) grown in vitro.
2003-08
Flumioxazin soil persistence and mineralization in laboratory experiments.
2003-07-30
Effects of flumioxazin herbicide on carbon nutrition of Vitis vinifera L.
2003-07-02
Impact of flumioxazin herbicide on growth and carbohydrate physiology in Vitis vinifera L.
2003-04
Photosynthetic responses of Lemna minor exposed to xenobiotics, copper, and their combinations.
2002-11
A plastidic ABC protein involved in intercompartmental communication of light signaling.
2001-01-01
Interorganellar crosstalk: new perspectives on signaling from the chloroplast to the nucleus.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:37:00 GMT 2025
Edited
by admin
on Mon Mar 31 19:37:00 GMT 2025
Record UNII
L0PX7OGI22
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUMIOXAZIN
HSDB   ISO   MI  
Common Name English
SUMISOYA
Preferred Name English
S-53482
Code English
N-(7-FLUORO-3,4-DIHYDRO-3-OXO-4-PROP-2-YNYL-2H-1,4-BENZOXAZIN-6-YL)CYCLOHEX-1-ENE-1,2-DICARBOXAMIDE
Systematic Name English
FLUMIOXAZIN [HSDB]
Common Name English
VALOR
Brand Name English
2-(7-FLUORO-3,4-DIHYDRO-3-OXO-4-(2-PROPYNYL)-2H-1,4-BENZOXAZIN-6-YL)-4,5,6,7-TETRAHYDRO-1H-ISOINDOLE-1,3(2H)-DIONE
Systematic Name English
V-53482
Code English
FLUMIOXAZIN [ISO]
Common Name English
FLUMIOXAZIN [MI]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 129034
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
Code System Code Type Description
FDA UNII
L0PX7OGI22
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
MESH
C106487
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
MERCK INDEX
m5444
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY Merck Index
PUBCHEM
92425
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
SMS_ID
300000052858
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
HSDB
7012
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
CHEBI
8939
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
ALANWOOD
flumioxazin
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
EPA CompTox
DTXSID7032555
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY
CAS
103361-09-7
Created by admin on Mon Mar 31 19:37:00 GMT 2025 , Edited by admin on Mon Mar 31 19:37:00 GMT 2025
PRIMARY