CHEBI:34620 - quinomethionate

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ChEBI Name quinomethionate
ChEBI ID CHEBI:34620
Definition A dithioloquinoxaline that results from the formal condensation of 6-methylquinoxaline-2,3-dithiol with phosgene. It has been used as a fungicide and acaricide for the control of mites and powdery mildew on citrus, vegetables, and walnuts, but is not approved for use in the EU.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C10H6N2OS2
Net Charge 0
Average Mass 234.29952
Monoisotopic Mass 233.99216
InChI InChI=1S/C10H6N2OS2/c1-5-2-3-6-7(4-5)12-9-8(11-6)14-10(13)15-9/h2-4H,1H3
InChIKey FBQQHUGEACOBDN-UHFFFAOYSA-N
SMILES Cc1ccc2nc3sc(=O)sc3nc2c1
Roles Classification
Application(s): agrochemical
An agrochemical is a substance that is used in agriculture or horticulture.
acaricide
A substance used to destroy pests of the subclass Acari (mites and ticks).
(via organonitrogen acaricide )
pesticide
Strictly, a substance intended to kill pests. In common usage, any substance used for controlling, preventing, or destroying animal, microbiological or plant pests.
(via organonitrogen pesticide )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing quinomethionate (CHEBI:34620) has role agrochemical (CHEBI:33286)
quinomethionate (CHEBI:34620) is a dithioloquinoxaline (CHEBI:38919)
quinomethionate (CHEBI:34620) is a quinoxaline acaricide (CHEBI:38820)
quinomethionate (CHEBI:34620) is a quinoxaline antifungal agent (CHEBI:38819)
IUPAC Name
6-methyl[1,3]dithiolo[4,5-b]quinoxalin-2-one
Synonyms Sources
6-methyl-2,3-quinoxalinedithiol cyclic dithiocarbonate NIST Chemistry WebBook
6-Methyl-2,3-quinoxalinedithiol cyclic S,S-dithiocarbonate KEGG COMPOUND
Chinomethionat KEGG COMPOUND
chinomethionate NIST Chemistry WebBook
oxythioquinox ChemIDplus
Quinomethionate KEGG COMPOUND
S,S-(6-methylquinoxaline-2,3-diyl) dithiocarbonate ChemIDplus
Brand Name Source
Morestan ChEBI
Manual Xrefs Databases
127 PPDB
C14514 KEGG COMPOUND
chinomethionat Alan Wood's Pesticides
View more database links
Registry Numbers Types Sources
2439-01-2 CAS Registry Number NIST Chemistry WebBook
2439-01-2 CAS Registry Number ChemIDplus
526833 Beilstein Registry Number Beilstein
526833 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
1009998 PubMed citation Europe PMC
14505671 PubMed citation Europe PMC
6658821 PubMed citation Europe PMC
IND84001481 Agricola citation Europe PMC
IND84001482 Agricola citation Europe PMC
Last Modified
01 September 2014