Record Information
Version1.0
Creation Date2016-06-03 11:32:33 UTC
Update Date2016-11-09 01:23:02 UTC
Accession NumberCHEM044000
Identification
Common Name4-Nitrobenzolsulfonsäure
ClassSmall Molecule
DescriptionNot Available
Contaminant Sources
  • STOFF IDENT Compounds
Contaminant TypeNot Available
Chemical Structure
Thumb
Synonyms
ValueSource
4-Nitrobenzene-1-sulfonateGenerator
4-Nitrobenzene-1-sulphonateGenerator
4-Nitrobenzene-1-sulphonic acidGenerator
4-NitrobenzenesulfonateMeSH, Generator
4-Nitrobenzenesulfonate potassium saltMeSH
P-NBSMeSH
Para-nitrobenzenesulfonateMeSH
4-NITROBENZENEsulphonateGenerator
4-NITROBENZENEsulphonic acidGenerator
Chemical FormulaC6H5NO5S
Average Molecular Mass203.170 g/mol
Monoisotopic Mass202.989 g/mol
CAS Registry Number138-42-1
IUPAC Name4-nitrobenzene-1-sulfonic acid
Traditional Name4-nitrobenzenesulfonic acid
SMILESOS(=O)(=O)C1=CC=C(C=C1)N(=O)=O
InChI IdentifierInChI=1S/C6H5NO5S/c8-7(9)5-1-3-6(4-2-5)13(10,11)12/h1-4H,(H,10,11,12)
InChI KeySPXOTSHWBDUUMT-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as p-nitrobenzenesulfonates. These are benzenesulfonic acids (or derivative thereof) carrying a nitro group at the para- position.
KingdomOrganic compounds
Super ClassBenzenoids
ClassBenzene and substituted derivatives
Sub ClassBenzenesulfonic acids and derivatives
Direct Parentp-Nitrobenzenesulfonates
Alternative Parents
Substituents
  • P-nitrobenzenesulfonate
  • P-bromobenzenesulfonate
  • Arylsulfonic acid or derivatives
  • Nitrobenzene
  • Benzenesulfonyl group
  • 1-sulfo,2-unsubstituted aromatic compound
  • Nitroaromatic compound
  • Organosulfonic acid or derivatives
  • Organic sulfonic acid or derivatives
  • Organosulfonic acid
  • Sulfonyl
  • C-nitro compound
  • Organic nitro compound
  • Allyl-type 1,3-dipolar organic compound
  • Propargyl-type 1,3-dipolar organic compound
  • Organic 1,3-dipolar compound
  • Organic oxoazanium
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Organosulfur compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Organic oxygen 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 Solubility0.9 g/LALOGPS
logP-0.87ALOGPS
logP1.09ChemAxon
logS-2.4ALOGPS
pKa (Strongest Acidic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area100.19 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity44.01 m³·mol⁻¹ChemAxon
Polarizability16.67 ųChemAxon
Number of Rings1ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0udi-0090000000-424e3b309974ab12d42fSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0k9i-0940000000-ac4e6b0b61da62df99c1Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03di-9800000000-41c49698075bf890f353Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-0090000000-d800ccbe13e2073ed17aSpectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0udi-0090000000-c14ac43d06dd1bf3cd00Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0udi-3090000000-9a8067674a1b5ddffdefSpectrum
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 ID8740
Kegg Compound IDNot Available
YMDB IDNot Available
ECMDB IDNot Available
References
Synthesis ReferenceNot Available
MSDSNot Available
General ReferencesNot Available