Record Information
Version1.0
Creation Date2016-05-22 03:41:48 UTC
Update Date2016-11-09 01:15:27 UTC
Accession NumberCHEM016732
Identification
Common NameIocetamic acid
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • STOFF IDENT Compounds
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
CholebrineKegg
3-[N-(3-Amino-2,4,6-triiodophenyl)acetamido]-2-methylpropanoateGenerator
3-(N-Acetyl-3-amino-2,4,6-triiodoanilino)-2-methylpropanoateGenerator
N-Acetyl-N-(3-amino-2,4,6-triiodophenyl)-2-methyl-beta-alanineMeSH
Iocetamic acidMeSH
Chemical FormulaC12H13I3N2O3
Average Molecular Mass613.960 g/mol
Monoisotopic Mass613.806 g/mol
CAS Registry Number16034-77-8
IUPAC Name3-[N-(3-amino-2,4,6-triiodophenyl)acetamido]-2-methylpropanoic acid
Traditional Nameiocetamic acid
SMILESCC(CN(C(C)=O)C1=C(I)C=C(I)C(N)=C1I)C(O)=O
InChI IdentifierInChI=1S/C12H13I3N2O3/c1-5(12(19)20)4-17(6(2)18)11-8(14)3-7(13)10(16)9(11)15/h3,5H,4,16H2,1-2H3,(H,19,20)
InChI KeyGSVQIUGOUKJHRC-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as o-haloacetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group, which is in turn ortho-substituted with a halogen atom.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassAnilides
Direct ParentO-haloacetanilides
Alternative Parents
Substituents
  • O-haloacetanilide
  • P-haloacetanilide
  • Aniline or substituted anilines
  • Halobenzene
  • Iodobenzene
  • Aryl halide
  • Aryl iodide
  • Acetamide
  • Tertiary carboxylic acid amide
  • Amino acid or derivatives
  • Carboxamide group
  • Amino acid
  • Carboxylic acid derivative
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Organohalogen compound
  • Primary amine
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Amine
  • Organic oxide
  • Carbonyl group
  • Organopnictogen compound
  • Organic oxygen compound
  • Organoiodide
  • Organonitrogen compound
  • Organooxygen 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 Solubility0.054 g/LALOGPS
logP3.15ALOGPS
logP2.99ChemAxon
logS-4.1ALOGPS
pKa (Strongest Acidic)2.74ChemAxon
pKa (Strongest Basic)1.58ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area83.63 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity104.18 m³·mol⁻¹ChemAxon
Polarizability40.06 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-03ds-4000096000-f15f1b51e67e402bdd82Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00tv-5000091000-bd6013c9ec0a75f15427Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-9000020000-538d1cb42c1b3c45383eSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-03di-0000059000-f734c29d5daea2c07a8dSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-047l-1000392000-391552c52ec2108eb8a5Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-003r-1000690000-d545c2ac5e0c93c7dd63Spectrum
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 ID27648
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available