Structure via PubChem · Public domain (PubChem)
linuron
Sign in to saveAlso known as N'-(3,4-dichlorophenyl)-N-methoxy-N-methyl Urea, 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea, 1-methoxy-1-methyl-3-(3,4-dichlorophenyl)urea
chemische verbinding
In the Vinony graph
Vinony's link graph records 673 inbound references to linuron, and connects out to phenoxy herbicide, abiraterone acetate and diuron.
It sits within the topics Chemical pages without DrugBank identifier, Drugs missing an ATC code and Drugs with no legal status.
Vinony links it to 9 Wikipedia language editions.
Chemical data
- Formula
- C9H10Cl2N2O2
- Molecular weight
- 249.09 g/mol
- IUPAC name
- 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea
- SMILES
- CN(C(=O)NC1=CC(=C(C=C1)Cl)Cl)OC
- InChIKey
- XKJMBINCVNINCA-UHFFFAOYSA-N
- XLogP
- 3.2
- Polar surface area
- 41.6 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
575 papers- Linuron and monolinuron.Residue reviews · 1981
- In vitro antiandrogenic effects of the herbicide linuron and its metabolites.Chemosphere · 2024
- Prenatal linuron exposure disrupts adrenal steroidogenesis and induces adrenal insufficiency in male rat offspring.Current research in toxicology · 2025
- DNA-SIP and repeated isolation corroborate Variovorax as a key organism in maintaining the genetic memory for linuron biodegradation in an agricultural soil.FEMS microbiology ecology · 2021
- Characterization of a Linuron-Specific Amidohydrolase from the Newly Isolated Bacterium Sphingobium sp. Strain SMB.Journal of agricultural and food chemistry · 2020
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 248.012
- Has use
- herbicide
Show 4 more facts
- chemical formula
- C₉H₁₀Cl₂N₂O₂
- canonical SMILES
- CN(C(=O)NC1=CC(=C(C=C1)Cl)Cl)OC
- isomeric SMILES
- CN(/C(=N\C1=CC=C(C(=C1)Cl)Cl)/O)OC
- Commons category
- Linuron
via Wikidata · CC0
Article · Nederlands
Linuron (ISO-naam) is een herbicide dat in veel verschillende teelten gebruikt wordt voor de bestrijding van eenjarige tweezaadlobbige onkruiden, zoals herderstasje, muur, kamille, zwarte nachtschade, wilgeroosje, basterdwederik en klein kruiskruid. Linuron behoort, zoals onder andere diuron en , tot de fenylureum-herbiciden. De stof werd tijdens de jaren '40 van de 20e eeuw ontwikkeld door het Amerikaanse E.I. du Pont de Nemours & Co. Handelsnamen van de stof zijn onder andere Lorox, Afalon, Linugan, Linurex, Linuron 450 Protex en Luxan Linuron.
Abstract from DBpedia / Wikipedia · CC BY-SA