Record Information
Version1.0
Creation Date2016-05-22 05:38:36 UTC
Update Date2016-11-09 01:15:53 UTC
Accession NumberCHEM018895
Identification
Common NameTenonitrozole
ClassSmall Molecule
Description
Contaminant Sources
  • ToxCast & Tox21 Chemicals
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
AtricanKegg
2-(alpha-Thenoylamino)-5-nitrothiazoleMeSH
2-(alpha-Thenoylamino)-2-nitro-5-thiazoleMeSH
Chemical FormulaC8H5N3O3S2
Average Molecular Mass255.270 g/mol
Monoisotopic Mass254.977 g/mol
CAS Registry Number3810-35-3
IUPAC NameN-(5-nitro-1,3-thiazol-2-yl)thiophene-2-carboxamide
Traditional Nameatrican
SMILESO=C(NC1=NC=C(S1)N(=O)=O)C1=CC=CS1
InChI IdentifierInChI=1S/C8H5N3O3S2/c12-7(5-2-1-3-15-5)10-8-9-4-6(16-8)11(13)14/h1-4H,(H,9,10,12)
InChI KeyZLOXYEZYWCTXHU-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as nitrothiazoles. Nitrothiazoles are compounds containing a thiazole ring which bears a nitro group.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassAzoles
Sub ClassThiazoles
Direct ParentNitrothiazoles
Alternative Parents
Substituents
  • 2-heteroaryl carboxamide
  • Nitroaromatic compound
  • Nitrothiazole
  • Thiophene carboxamide
  • Thiophene carboxylic acid or derivatives
  • 2,5-disubstituted 1,3-thiazole
  • Heteroaromatic compound
  • Thiophene
  • Carboxamide group
  • C-nitro compound
  • Secondary carboxylic acid amide
  • Organic nitro compound
  • Carboxylic acid derivative
  • Organic oxoazanium
  • Azacycle
  • Organic 1,3-dipolar compound
  • Propargyl-type 1,3-dipolar organic compound
  • Allyl-type 1,3-dipolar organic compound
  • Organooxygen compound
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Organic nitrogen compound
  • Organopnictogen compound
  • Organic zwitterion
  • Organic oxide
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic 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 Solubility0.21 g/LALOGPS
logP2.13ALOGPS
logP2.43ChemAxon
logS-3.1ALOGPS
pKa (Strongest Acidic)10.08ChemAxon
pKa (Strongest Basic)-4.2ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area87.81 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity59.65 m³·mol⁻¹ChemAxon
Polarizability22.93 ųChemAxon
Number of Rings2ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0a4i-0090000000-7299412cf9f8e1ffaa1eSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0zfr-0090000000-6969e0c65e0f38ecc8acSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-002b-9200000000-8e3679730eeec8da6e01Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-1190000000-97c4882ff7932b9570d1Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0zmi-9250000000-4e30ac79e3eda5ec81afSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a4i-9000000000-9878fc35ac9412ef96cfSpectrum
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 IDDB13659
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 LinkTenonitrozole
Chemspider IDNot Available
ChEBI IDNot Available
PubChem Compound ID19646
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available