Record Information
Version1.0
Creation Date2016-05-19 02:39:01 UTC
Update Date2016-11-09 01:13:44 UTC
Accession NumberCHEM008134
Identification
Common NameBifenox
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • My Exposome Chemicals
  • STOFF IDENT Compounds
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
MC-4379Kegg
Methyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoic acidGenerator
2,4-Dichlorophenyl-3'-carboxymethyl-4'-nitrophenyl etherMeSH
BifenoxMeSH
Chemical FormulaC14H9Cl2NO5
Average Molecular Mass342.130 g/mol
Monoisotopic Mass340.986 g/mol
CAS Registry Number42576-02-3
IUPAC Namemethyl 5-(2,4-dichlorophenoxy)-2-nitrobenzoate
Traditional Namemodown
SMILESCOC(=O)C1=C(C=CC(OC2=C(Cl)C=C(Cl)C=C2)=C1)N(=O)=O
InChI IdentifierInChI=1S/C14H9Cl2NO5/c1-21-14(18)10-7-9(3-4-12(10)17(19)20)22-13-5-2-8(15)6-11(13)16/h2-7H,1H3
InChI KeySUSRORUBZHMPCO-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as diphenylethers. These are aromatic compounds containing two benzene rings linked to each other through an ether group.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassDiphenylethers
Direct ParentDiphenylethers
Alternative Parents
Substituents
  • Diphenylether
  • Nitrobenzoate
  • Diaryl ether
  • Benzoate ester
  • Benzoic acid or derivatives
  • Nitrobenzene
  • Phenoxy compound
  • Nitroaromatic compound
  • Benzoyl
  • 1,3-dichlorobenzene
  • Phenol ether
  • Chlorobenzene
  • Halobenzene
  • Aryl chloride
  • Aryl halide
  • Methyl ester
  • Carboxylic acid ester
  • Organic nitro compound
  • C-nitro compound
  • Organic oxoazanium
  • Carboxylic acid derivative
  • Organic 1,3-dipolar compound
  • Monocarboxylic acid or derivatives
  • Allyl-type 1,3-dipolar organic compound
  • Ether
  • Propargyl-type 1,3-dipolar organic compound
  • Organochloride
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Organohalogen compound
  • Organonitrogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Biological Properties
StatusDetected and Not Quantified
OriginNot Available
Cellular LocationsNot Available
Biofluid LocationsNot Available
Tissue LocationsNot Available
PathwaysNot Available
ApplicationsNot Available
Biological RolesNot Available
Chemical RolesNot Available
Physical Properties
StateNot Available
AppearanceNot Available
Experimental Properties
PropertyValue
Melting PointNot Available
Boiling PointNot Available
SolubilityNot Available
Predicted Properties
PropertyValueSource
Water Solubility0.00049 g/LALOGPS
logP4.31ALOGPS
logP4.63ChemAxon
logS-5.8ALOGPS
pKa (Strongest Basic)-3.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area81.35 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity81.26 m³·mol⁻¹ChemAxon
Polarizability30.35 ųChemAxon
Number of Rings2ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0009000000-ab608f7f5dcbb31595fbSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-0009000000-1f3d7b1e23d5e03df885Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0udi-0922000000-2f77c53540b3461f4ad9Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-000i-0009000000-d27ca9893c7c4bab560aSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-000i-0009000000-7189e50d047e71a4a7beSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0296-1893000000-d1b69a29d2e1673ff08bSpectrum
Toxicity Profile
Route of ExposureNot Available
Mechanism of ToxicityNot Available
MetabolismNot Available
Toxicity ValuesNot Available
Lethal DoseNot Available
Carcinogenicity (IARC Classification)Not Available
Uses/SourcesNot Available
Minimum Risk LevelNot Available
Health EffectsNot Available
SymptomsNot Available
TreatmentNot Available
Concentrations
Not Available
DrugBank IDNot Available
HMDB IDNot Available
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkNot Available
Chemspider IDNot Available
ChEBI IDNot Available
PubChem Compound ID39230
Kegg Compound IDC11066
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available