Basic Info

Common NameFenoprop(F06002)
2D Structure
FRCD IDF06002
CAS Number93-72-1
PubChem CID7158
FormulaC9H7Cl3O3
IUPAC Name

2-(2,4,5-trichlorophenoxy)propanoic acid

InChI Key

ZLSWBLPERHFHIS-UHFFFAOYSA-N

InChI

InChI=1S/C9H7Cl3O3/c1-4(9(13)14)15-8-3-6(11)5(10)2-7(8)12/h2-4H,1H3,(H,13,14)

Canonical SMILES

CC(C(=O)O)OC1=CC(=C(C=C1Cl)Cl)Cl

Isomeric SMILES

CC(C(=O)O)OC1=CC(=C(C=C1Cl)Cl)Cl

Synonyms
        
            2-(2,4,5-Trichlorophenoxy)propionic acid
        
            Fenoprop
        
            SILVEX
        
            93-72-1
        
            Double strength
        
            Fenormone
        
            Propon
        
            Color-set
        
            Aqua-vex
        
            Sta-fast
        
Classifies
                

                  
                    Pesticide
                  

                
        
Update DateNov 13, 2018 17:07

Chemical Taxonomy

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
Subclass2-phenoxypropionic acids
Intermediate Tree NodesNot available
Direct Parent2-phenoxypropionic acids
Alternative Parents
Molecular FrameworkAromatic homomonocyclic compounds
Substituents2-phenoxypropionic acid - Phenoxyacetate - Phenoxy compound - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Carbonyl group - Organic oxide - Organochloride - Hydrocarbon derivative - Organohalogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 2-phenoxypropionic acids. These are aromatic compounds hat contain a phenol ether attached to the C2-atom of a phenylpropionic acid.

Properties

Property NameProperty Value
Molecular Weight269.502
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count3
Complexity237
Monoisotopic Mass267.946
Exact Mass267.946
XLogP3.8
Formal Charge0
Heavy Atom Count15
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

ADMET

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.8966
Human Intestinal AbsorptionHIA+0.9929
Caco-2 PermeabilityCaco2+0.7753
P-glycoprotein SubstrateNon-substrate0.7069
P-glycoprotein InhibitorNon-inhibitor0.9440
Non-inhibitor0.9736
Renal Organic Cation TransporterNon-inhibitor0.9098
Distribution
Subcellular localizationMitochondria0.9380
Metabolism
CYP450 2C9 SubstrateNon-substrate0.7431
CYP450 2D6 SubstrateNon-substrate0.9091
CYP450 3A4 SubstrateNon-substrate0.6241
CYP450 1A2 InhibitorNon-inhibitor0.7903
CYP450 2C9 InhibitorNon-inhibitor0.8533
CYP450 2D6 InhibitorNon-inhibitor0.9427
CYP450 2C19 InhibitorNon-inhibitor0.8849
CYP450 3A4 InhibitorNon-inhibitor0.9504
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8787
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9671
Non-inhibitor0.9507
AMES ToxicityNon AMES toxic0.9484
CarcinogensNon-carcinogens0.8058
Fish ToxicityHigh FHMT0.9485
Tetrahymena Pyriformis ToxicityHigh TPT0.9674
Honey Bee ToxicityHigh HBT0.7350
BiodegradationNot ready biodegradable0.8085
Acute Oral ToxicityIII0.8573
Carcinogenicity (Three-class)Non-required0.4716

Model Value Unit
Absorption
Aqueous solubility-2.3374LogS
Caco-2 Permeability1.0579LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity2.6172LD50, mol/kg
Fish Toxicity0.5871pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.1358pIGC50, ug/L

MRLs

FoodProduct CodeCountryMRLsApplication DateNotes
Mineral WatersJapan0.009ppm
SimazineAustralia0.02mg/kg
ApplesAustralia0.02mg/kg