CHEBI:59246 - sulcofuron

ChEBI IDCHEBI:59246
ChEBI Namesulcofuron
Stars
DefinitionAn organochlorine pesticide consisting of 1,3-diphenylurea having chloro substituents at the 3-, 4- and 5'-positions and a 4-chloro-2-sulfophenoxy group at the 2'-position.
Last Modified10 December 2016
SubmitterSteve
DownloadsMolfile
FormulaC19H12Cl4N2O5S
Net Charge0
Average Mass522.193
Monoisotopic Mass519.92210
SMILESO=C(Nc1ccc(Cl)c(Cl)c1)Nc1cc(Cl)ccc1Oc1ccc(Cl)cc1S(=O)(=O)O
InChIInChI=1S/C19H12Cl4N2O5S/c20-10-1-5-16(30-17-6-2-11(21)8-18(17)31(27,28)29)15(7-10)25-19(26)24-12-3-4-13(22)14(23)9-12/h1-9H,(H2,24,25,26)(H,27,28,29)
InChIKeyMKUMTCOTMQPYTQ-UHFFFAOYSA-N
Roles Classification
Biological Role:
epitope  The biological role played by a material entity when bound by a receptor of the adaptive immune system. Specific site on an antigen to which an antibody binds.
Applications:
insecticide  Strictly, a substance intended to kill members of the class Insecta. In common usage, any substance used for preventing, destroying, repelling or controlling insects.
pesticide  Strictly, a substance intended to kill pests. In common usage, any substance used for controlling, preventing, or destroying animal, microbiological or plant pests.
ChEBI Ontology
Outgoing Relation(s)
sulcofuron (CHEBI:59246) has functional parent 1,3-diphenylurea (CHEBI:41320)
sulcofuron (CHEBI:59246) has role epitope (CHEBI:53000)
sulcofuron (CHEBI:59246) has role insecticide (CHEBI:24852)
sulcofuron (CHEBI:59246) is a arenesulfonic acid (CHEBI:33555)
sulcofuron (CHEBI:59246) is a dichlorobenzene (CHEBI:23697)
sulcofuron (CHEBI:59246) is a organochlorine pesticide (CHEBI:38656)
sulcofuron (CHEBI:59246) is a phenylureas (CHEBI:134043)
sulcofuron (CHEBI:59246) is conjugate acid of sulcofuronate (CHEBI:59248)
Incoming Relation(s)
sulcofuronate (CHEBI:59248) is conjugate base of sulcofuron (CHEBI:59246)
IUPAC Name 
5-chloro-2-(4-chloro-2-{[(3,4-dichlorophenyl)carbamoyl]amino}phenoxy)benzene-1-sulfonic acid
Manual XrefsDatabases
sulcofuronAlan Wood's Pesticides
US5912270Patent
Registry NumbersSources
Reaxys:3517243Reaxys
CAS:24019-05-4ChemIDplus
Citations