Record Information
Version1.0
Creation Date2016-06-03 11:25:01 UTC
Update Date2026-03-25 19:23:36 UTC
Accession NumberCHEM043899
Identification
Common NameCycloxydim
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • STOFF IDENT Compounds
Contaminant TypeNot Available
Chemical Structure
SynonymsNot Available
Chemical FormulaC17H27NO3S
Average Molecular Mass325.470 g/mol
Monoisotopic Mass325.171 g/mol
CAS Registry Number101205-02-1
IUPAC Name2-[1-(ethoxyamino)butylidene]-5-(thian-3-yl)cyclohexane-1,3-dione
Traditional Name2-[1-(ethoxyamino)butylidene]-5-(thian-3-yl)cyclohexane-1,3-dione
SMILESCCCC(NOCC)=C1C(=O)CC(CC1=O)C1CCCSC1
InChI IdentifierInChI=1S/C17H27NO3S/c1-3-6-14(18-21-4-2)17-15(19)9-13(10-16(17)20)12-7-5-8-22-11-12/h12-13,18H,3-11H2,1-2H3/b17-14-
InChI KeyHAHCNFVGRVWFIP-VKAVYKQESA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as thianes. These are heterocyclic compounds containing a saturated six-member ring with five carbon atoms and one sulfur atom.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassThianes
Sub ClassNot Available
Direct ParentThianes
Alternative Parents
Substituents
  • Thiane
  • Vinylogous amide
  • Cyclic ketone
  • Ketone
  • N-organohydroxylamine
  • Dialkylthioether
  • Thioether
  • Organic nitrogen compound
  • Organic oxygen compound
  • Organopnictogen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organonitrogen compound
  • Carbonyl group
  • 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 Solubility0.07 g/LALOGPS
logP3.1ALOGPS
logP3.09ChemAxon
logS-3.7ALOGPS
pKa (Strongest Acidic)17.3ChemAxon
pKa (Strongest Basic)-4.5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area55.4 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity102.53 m³·mol⁻¹ChemAxon
Polarizability36.64 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
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 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 IDNot Available
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General References