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Details

Stereochemistry RACEMIC
Molecular Formula C13H18O5S
Molecular Weight 286.344
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHOFUMESATE

SMILES

CCOC1OC2=CC=C(OS(C)(=O)=O)C=C2C1(C)C

InChI

InChIKey=IRCMYGHHKLLGHV-UHFFFAOYSA-N
InChI=1S/C13H18O5S/c1-5-16-12-13(2,3)10-8-9(18-19(4,14)15)6-7-11(10)17-12/h6-8,12H,5H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C13H18O5S
Molecular Weight 286.344
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Species differences for stereoselective metabolism of ethofumesate and its enantiomers in vitro.
2009-09
2-Acetyl-hydrazono-2-phenyl-aceto-hydrazide.
2008-08-23
Method development for the determination of selected pesticides on tobacco by high-performance liquid chromatography-electrospray ionisation-tandem mass spectrometry.
2008-02-15
Ethyl 2-acetyl-hydrazono-2-phenyl-acetate.
2007-12-06
Stereoselective toxicokinetics and tissue distribution of ethofumesate in rabbits.
2007-08
Fate of the herbicides glyphosate, glufosinate-ammonium, phenmedipham, ethofumesate and metamitron in two Finnish arable soils.
2006-06
Enantiomeric resolution of chiral pesticides by high-performance liquid chromatography.
2006-03-08
Use of growth regulator of cytokinin type for enhancement and modification of herbicide activity.
2006
Adsorption of sugar beet herbicides to Finnish soils.
2004-04
Determination of herbicides, including thermally labile phenylureas, by solid-phase microextraction and gas chromatography-mass spectrometry.
2003-06-20
A qualitative sampling method for monitoring water quality in temporary channels or point sources and its application to pesticide contamination.
2003-05
Solid-phase extraction and sample stacking-micellar electrokinetic capillary chromatography for the determination of multiresidues of herbicides and metabolites.
2003-03-21
Mobility and dissipation of ethofumesate and halofenozide in turfgrass and bare soil.
2001-06
Effects of vapours of chlorpropham and ethofumesate on wild plant species.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:09:32 GMT 2025
Edited
by admin
on Mon Mar 31 22:09:32 GMT 2025
Record UNII
3051U1Z8KV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHOFUMESATE
HSDB   ISO   MI  
Common Name English
BURAKOSAT
Preferred Name English
KEMIRON PLUS
Brand Name English
2-ETHOXY-2,3-DIHYDRO-3,3-DIMETHYL-5-BENZOFURANYL METHANESULFONATE
Systematic Name English
5-BENZOFURANOL, 2-ETHOXY-2,3-DIHYDRO-3,3-DIMETHYL-, 5-METHANESULFONATE
Systematic Name English
ETHOSAT
Common Name English
2,3-DIHYDRO-3,3-DIMETHYL-2-ETHOXY-5-BENZOFURANYL METHANESULFONATE, (±)-
Systematic Name English
2-ETHOXY-2,3-DIHYDRO-3,3-DIMETHYL-5-BENZOFURANYL METHANESULFONATE, (±)-
Systematic Name English
ETHOFUMESATE [ISO]
Common Name English
ETHOFUMESATE [HSDB]
Common Name English
5-BENZOFURANOL, 2-ETHOXY-2,3-DIHYDRO-3,3-DIMETHYL-, METHANESULFONATE
Systematic Name English
5-BENZOFURANOL, 2-ETHOXY-2,3-DIHYDRO-3,3-DIMETHYL-, METHANESULFONATE, (±)-
Systematic Name English
ETHOFUMESATE [MI]
Common Name English
2-ETHOXY-2,3-DIHYDRO-3,3-DIMETHYLBENZOFURAN-5-YL METHANESULPHONATE, (±)-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 110601
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
Code System Code Type Description
PUBCHEM
33360
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY
MERCK INDEX
m5066
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY Merck Index
HSDB
7451
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY
EPA CompTox
DTXSID8034580
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY
ALANWOOD
ethofumesate
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY
ECHA (EC/EINECS)
247-525-3
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY
CAS
26225-79-6
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY
FDA UNII
3051U1Z8KV
Created by admin on Mon Mar 31 22:09:32 GMT 2025 , Edited by admin on Mon Mar 31 22:09:32 GMT 2025
PRIMARY