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Details

Stereochemistry ACHIRAL
Molecular Formula C14H17N5O7S2
Molecular Weight 431.444
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIMSULFURON

SMILES

CCS(=O)(=O)C1=C(N=CC=C1)S(=O)(=O)NC(=O)NC2=NC(OC)=CC(OC)=N2

InChI

InChIKey=MEFOUWRMVYJCQC-UHFFFAOYSA-N
InChI=1S/C14H17N5O7S2/c1-4-27(21,22)9-6-5-7-15-12(9)28(23,24)19-14(20)18-13-16-10(25-2)8-11(17-13)26-3/h5-8H,4H2,1-3H3,(H2,16,17,18,19,20)

HIDE SMILES / InChI

Molecular Formula C14H17N5O7S2
Molecular Weight 431.444
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Environmental impact on vascular development predicted by high-throughput screening.
2011-11
Biodegradation of chlorimuron-ethyl by the bacterium Klebsiella jilinsis 2N3.
2010-08
Trace determination of sulfonylurea herbicides in water and grape samples by capillary zone electrophoresis using large volume sample stacking.
2010-07
Long-term leaching of rimsulfuron degradation products through sandy agricultural soils.
2010-05
N-methylimidazolium ionic liquid-functionalized silica as a sorbent for selective solid-phase extraction of 12 sulfonylurea herbicides in environmental water and soil samples.
2010-03-05
Leaching of three sulfonylurea herbicides during sprinkler irrigation.
2010-01-06
Trace level determination of selected sulfonylurea herbicides in wetland sediment by liquid chromatography electrospray tandem mass spectrometry.
2010-01
The watershed as a conceptual framework for the study of environmental and human health.
2009-02-18
Development and validation of a multi-residue method for pesticide determination in honey using on-column liquid-liquid extraction and liquid chromatography-tandem mass spectrometry.
2007-06-08
HPLC-UV and HPLC-MSn multiresidue determination of amidosulfuron, azimsulfuron, nicosulfuron, rimsulfuron, thifensulfuron methyl, tribenuron methyl and azoxystrobin in surface waters.
2006-10-10
Herbicide resistance in Aster squamatus conferred by a less sensitive form of acetolactate synthase.
2003-11
Dissipation of nicosulfuron and rimsulfuron in surface soil.
2002-07-31
Measurement of xylem translocation of weak electrolytes with the pressure chamber technique.
2002-05
Nicosulfuron: alcoholysis, chemical hydrolysis, and degradation on various minerals.
2002-01-30
Simultaneous determination of binary mixtures of sulfonylurea herbicides in water by first-derivative photochemically induced spectrofluorimetry.
2002-01-05
Degradation in soil and water and ecotoxicity of rimsulfuron and its metabolites.
2001-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:07:40 GMT 2025
Edited
by admin
on Mon Mar 31 19:07:40 GMT 2025
Record UNII
462J071RD7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RIMSULFURON
ISO   MI  
Common Name English
1-(4,6-DIMETHOXYPYRIMIDIN-2-YL)-3-(3-ETHYLSULFONYL-2-PYRIDYLSULFONYL)UREA
Preferred Name English
DPX-E9636
Common Name English
RIMSULFURON [ISO]
Common Name English
RIMSULFURON [MI]
Common Name English
N-(((4,6-DIMETHOXY-2-PYRIMIDINYL)AMINO)CARBONYL)-3-(ETHYLSULFONYL)-2-PYRIDINESULFONAMIDE
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 129009
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
Code System Code Type Description
CAS
122931-48-0
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
PRIMARY
MERCK INDEX
m9626
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
PRIMARY Merck Index
PUBCHEM
91779
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
PRIMARY
HSDB
7947
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
PRIMARY
ALANWOOD
rimsulfuron
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
PRIMARY
FDA UNII
462J071RD7
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID1032642
Created by admin on Mon Mar 31 19:07:40 GMT 2025 , Edited by admin on Mon Mar 31 19:07:40 GMT 2025
PRIMARY