Record Information
Version1.0
Creation Date2016-06-03 12:27:06 UTC
Update Date2016-11-09 01:23:11 UTC
Accession NumberCHEM044651
Identification
Common NameTris{4-[(4-acetylphenyl)sulfanyl]phenyl}sulfonium hexafluorophosphate
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • STOFF IDENT Compounds
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
Hexafluoro--phosphanuide; tris({4-[(4-acetylphenyl)sulphanyl]phenyl})sulphaniumGenerator
Hexafluoro-λ⁵-phosphanuide
tris({4-[(4-acetylphenyl)sulphanyl]phenyl})sulphanium
Chemical FormulaC42H33F6O3PS4
Average Molecular Mass858.930 g/mol
Monoisotopic Mass858.095 g/mol
CAS Registry Number953084-13-4
IUPAC Namehexafluoro-lambda5-phosphanuide; tris({4-[(4-acetylphenyl)sulfanyl]phenyl})sulfanium
Traditional Namehexafluoro-lambda5-phosphanuide; tris({4-[(4-acetylphenyl)sulfanyl]phenyl})sulfanium
SMILESF[P-](F)(F)(F)(F)F.CC(=O)C1=CC=C(SC2=CC=C(C=C2)[S+](C2=CC=C(SC3=CC=C(C=C3)C(C)=O)C=C2)C2=CC=C(SC3=CC=C(C=C3)C(C)=O)C=C2)C=C1
InChI IdentifierInChI=1S/C42H33O3S4.F6P/c1-28(43)31-4-10-34(11-5-31)46-37-16-22-40(23-17-37)49(41-24-18-38(19-25-41)47-35-12-6-32(7-13-35)29(2)44)42-26-20-39(21-27-42)48-36-14-8-33(9-15-36)30(3)45;1-7(2,3,4,5)6/h4-27H,1-3H3;/q+1;-1
InChI KeyYXSHMKGGFIQDGA-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbonyl compounds
Direct ParentAlkyl-phenylketones
Alternative Parents
Substituents
  • Alkyl-phenylketone
  • Diarylthioether
  • Acetophenone
  • Aryl thioether
  • Benzoyl
  • Aryl alkyl ketone
  • Thiophenol ether
  • Monocyclic benzene moiety
  • Benzenoid
  • Sulfenyl compound
  • Thioether
  • Organic oxide
  • Organosulfur compound
  • Organic salt
  • Hydrocarbon derivative
  • 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 Solubility5.2e-05 g/LALOGPS
logP8.68ALOGPS
logP9.2ChemAxon
logS-7.2ALOGPS
pKa (Strongest Acidic)15.56ChemAxon
pKa (Strongest Basic)-6.9ChemAxon
Physiological Charge1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area51.21 ŲChemAxon
Rotatable Bond Count12ChemAxon
Refractivity211.44 m³·mol⁻¹ChemAxon
Polarizability79.98 ųChemAxon
Number of Rings6ChemAxon
Bioavailability0ChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Spectra
SpectraNot Available
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 IDNot Available
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available