Record Information
Version1.0
Creation Date2016-05-22 05:18:14 UTC
Update Date2026-04-06 13:25:42 UTC
Accession NumberCHEM018514
Identification
Common NameMifobate
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
ClenicorKegg
Dimethyl [(4-chlorophenyl)[(dimethoxyphosphoryl)oxy]methyl]phosphonic acidGenerator
[(4-Chlorophenyl)-dimethoxyphosphorylmethyl] dimethyl phosphoric acidGenerator
MifobateMeSH
(4-Chlorophenyl)(dimethoxyphosphinyl)methylphosphoric acid dimethyl esterMeSH
Dimethyl alpha-(dimethoxyphosphinyl)-4-chlorobenzyl phosphateMeSH
Mifobic acidGenerator
Chemical FormulaC11H17ClO7P2
Average Molecular Mass358.650 g/mol
Monoisotopic Mass358.014 g/mol
CAS Registry Number76541-72-5
IUPAC Namedimethyl [(4-chlorophenyl)[(dimethoxyphosphoryl)oxy]methyl]phosphonate
Traditional Namemifobate
SMILESCOP(=O)(OC)OC(C1=CC=C(Cl)C=C1)P(=O)(OC)OC
InChI IdentifierInChI=1S/C11H17ClO7P2/c1-15-20(13,16-2)11(19-21(14,17-3)18-4)9-5-7-10(12)8-6-9/h5-8,11H,1-4H3
InChI KeyVQHUQHAPWMNBLP-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as trialkyl phosphates. These are organic compounds containing a phosphate group that is linked to exactly three alkyl chains.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassOrganic phosphoric acids and derivatives
Sub ClassPhosphate esters
Direct ParentTrialkyl phosphates
Alternative Parents
Substituents
  • Trialkyl phosphate
  • Dialkyl alkylphosphonate
  • Chlorobenzene
  • Phosphonic acid diester
  • Halobenzene
  • Aryl chloride
  • Aryl halide
  • Monocyclic benzene moiety
  • Benzenoid
  • Phosphonic acid ester
  • Organophosphonic acid derivative
  • Organic oxygen compound
  • Organochloride
  • Organooxygen compound
  • Organohalogen compound
  • Organophosphorus compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organopnictogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
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 Solubility4.79 g/LALOGPS
logP1.6ALOGPS
logP2.78ChemAxon
logS-1.9ALOGPS
pKa (Strongest Basic)-8.2ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area80.29 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity76.89 m³·mol⁻¹ChemAxon
Polarizability30.49 ųChemAxon
Number of Rings1ChemAxon
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, Positivesplash10-0a4i-0009000000-01151912fe6cf746da7aSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a6r-0019000000-b33f19956d4532c9d830Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-001i-9026000000-e19ee461834ddf2e4d5aSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a4i-0009000000-0be2170675298e9c2431Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0abc-0029000000-1c1701f3fb095a5ec282Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0006-1191000000-7afb84498f49a9a84c27Spectrum
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 ID60910
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available