Record Information
Version1.0
Creation Date2016-05-19 01:42:06 UTC
Update Date2026-08-22 18:13:18 UTC
Accession NumberCHEM004351
Identification
Common Name2,2'-Bioxirane
ClassSmall Molecule
Description
Contaminant Sources
  • Clean Air Act Chemicals
  • HPV EPA Chemicals
  • IARC Carcinogens General
Contaminant TypeNot Available
Chemical Structure
Synonyms
ValueSource
1,1'-Bi[ethylene oxide]ChEBI
1,2:3,4-Butadiene diepoxideChEBI
1,2:3,4-DianhydrothreitolChEBI
1,2:3,4-DiepoxybutaneChEBI
1,3-Butadiene diepoxideChEBI
BioxiraneChEBI
ButadiendioxydChEBI
Butadiene diepoxideChEBI
Butadiene dioxideChEBI
Butane diepoxideChEBI
DEBChEBI
DioxybutadieneChEBI
1,2,3,4-DiepoxybutaneMeSH, HMDB
DiepoxybutaneMeSH, HMDB
Erythritol anhydride, (R-(r*,r*))-isomerMeSH, HMDB
Erythritol anhydride, (S-(r*,r*))-isomerMeSH, HMDB
Erythritol anhydride, (r*,s*)-isomerMeSH, HMDB
1,2-3,4-DiepoxybutaneMeSH, HMDB
Erythritol anhydrideMeSH, HMDB
Erythritol anhydride, ((r*,r*)-(+-))-isomerMeSH, HMDB
Butadiene bisoxideMeSH, HMDB
2,2'-BioxiraneMeSH
Chemical FormulaC4H6O2
Average Molecular Mass86.090 g/mol
Monoisotopic Mass86.037 g/mol
CAS Registry Number1464-53-5
IUPAC Name2,2'-bioxirane
Traditional Name2,2'-bioxirane
SMILESC1OC1C1CO1
InChI IdentifierInChI=1S/C4H6O2/c1-3(5-1)4-2-6-4/h3-4H,1-2H2
InChI KeyZFIVKAOQEXOYFY-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as epoxides. Epoxides are compounds containing a cyclic ether with three ring atoms(one oxygen and two carbon atoms).
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassEpoxides
Sub ClassNot Available
Direct ParentEpoxides
Alternative Parents
Substituents
  • Oxacycle
  • Ether
  • Oxirane
  • Dialkyl ether
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic 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 Solubility326 g/LALOGPS
logP-0.36ALOGPS
logP-0.15ChemAxon
logS0.58ALOGPS
pKa (Strongest Basic)-3.9ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area21.76 ŲChemAxon
Rotatable Bond Count1ChemAxon
Refractivity19.46 m³·mol⁻¹ChemAxon
Polarizability8.24 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
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
External Links
DrugBank IDNot Available
HMDB IDHMDB0251927
FooDB IDNot Available
Phenol Explorer IDNot Available
KNApSAcK IDNot Available
BiGG IDNot Available
BioCyc IDNot Available
METLIN IDNot Available
PDB IDNot Available
Wikipedia LinkDiepoxybutane
Chemspider ID21106504
ChEBI ID23704
PubChem Compound IDNot Available
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References