Record Information
Version1.0
Creation Date2016-05-19 04:58:22 UTC
Update Date2016-10-28 10:01:11 UTC
Accession NumberCHEM015710
Identification
Common NameMucochloric acid
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • Disinfection Byproducts
  • OECD HPV Chemicals
  • STOFF IDENT Compounds
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
3,4-Dichloro-5-hydroxy-2(5H)-furanoneMeSH
3,4-(Dichloro)-5-hydroxy-2(5H)-furanoneMeSH
3,4-MAMeSH
MCA CPDMeSH
Chemical FormulaC4H2Cl2O3
Average Molecular Mass168.960 g/mol
Monoisotopic Mass167.938 g/mol
CAS Registry Number87-56-9
IUPAC Name3,4-dichloro-5-hydroxy-2,5-dihydrofuran-2-one
Traditional Name3,4-dichloro-5-hydroxy-5H-furan-2-one
SMILESOC1OC(=O)C(Cl)=C1Cl
InChI IdentifierInChI=1S/C4H2Cl2O3/c5-1-2(6)4(8)9-3(1)7/h3,7H
InChI KeyZAKLKBFCSHJIRI-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassDihydrofurans
Sub ClassFuranones
Direct ParentButenolides
Alternative Parents
Substituents
  • 2-furanone
  • Vinylogous halide
  • Alpha,beta-unsaturated carboxylic ester
  • Enoate ester
  • Carboxylic acid ester
  • Chlorohydrin
  • Halohydrin
  • Hemiacetal
  • Lactone
  • Carboxylic acid derivative
  • Oxacycle
  • Chloroalkene
  • Haloalkene
  • Monocarboxylic acid or derivatives
  • Vinyl chloride
  • Vinyl halide
  • Carbonyl group
  • Organic oxide
  • Organohalogen compound
  • Organochloride
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic 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 Solubility49.7 g/LALOGPS
logP0.42ALOGPS
logP0.8ChemAxon
logS-0.53ALOGPS
pKa (Strongest Acidic)10.56ChemAxon
pKa (Strongest Basic)-4.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area46.53 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity31.78 m³·mol⁻¹ChemAxon
Polarizability12.37 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014l-4900000000-a7d49ca43dc026614b16Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-0900000000-ee5dc0406b19c1e2b84fSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-9100000000-6ce6b160376ecabed862Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014i-0900000000-2f2416d65997355dc0f6Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0159-0900000000-d234745b96f701d37a54Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-01c0-3900000000-4c4a5e5d235d634d6720Spectrum
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 ID91487
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available