Showing Compound Card for 1,2-Benzenediol, 3,4-dichloro- (CDB006102)

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Record Information
Version1.0
Created at2020-04-27 17:29:45 UTC
Updated at2021-01-06 19:07:03 UTC
CannabisDB IDCDB006102
Secondary Accession NumbersNot Available
Cannabis Compound Identification
Common Name1,2-Benzenediol, 3,4-dichloro-
Description3,4-Dichlorocatechol, also known as DCBZ or 1,2-Benzenediol, 3,4-dichloro-, belongs to the class of organic compounds known as 4-chlorocatechols. These are chlorocatechols with the chlorine atom attached at position C4 of the benzene ring. 3,4-Dichlorocatechol is an extremely weak basic (essentially neutral) compound (based on its pKa). A dichlorocatechol that is catechol in which the hydrogens at positions 3 and 4 are replaced by chlorines. 3,4-Dichlorocatechol is formed during the combustion of cannabis and is therefore a constituent of cannabis smoke ( Ref:DOI ).
Structure
Thumb
MOLSDF3D-SDFPDBSMILESInChI View 3D Structure
Synonyms
ValueSource
DCBZChEBI
3,4-Dichlorocatechol, dipotassium saltMeSH
3,4-Dichloro-1,2-benzenediolMeSH
3,4-DichlorocatecholMeSH
Chemical FormulaC6H4Cl2O2
Average Molecular Weight179.0
Monoisotopic Molecular Weight177.9588
IUPAC Name3,4-dichlorobenzene-1,2-diol
Traditional Name3,4-dichlorobenzene-1,2-diol
CAS Registry Number3978-67-4
SMILES
OC1=C(O)C(Cl)=C(Cl)C=C1
InChI Identifier
InChI=1S/C6H4Cl2O2/c7-3-1-2-4(9)6(10)5(3)8/h1-2,9-10H
InChI KeyHFSXRRTUWAPWSJ-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 4-chlorocatechols. These are chlorocatechols with the chlorine atom attached at position C4 of the benzene ring.
KingdomOrganic compounds
Super ClassBenzenoids
ClassPhenols
Sub ClassBenzenediols
Direct Parent4-chlorocatechols
Alternative Parents
Substituents
  • 3-chlorocatechol
  • 4-chlorocatechol
  • 4-chlorophenol
  • 1,2-dichlorobenzene
  • 2-chlorophenol
  • 3-chlorophenol
  • 2-halophenol
  • 3-halophenol
  • 4-halophenol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Chlorobenzene
  • Halobenzene
  • Aryl chloride
  • Aryl halide
  • Monocyclic benzene moiety
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Organooxygen compound
  • Organochloride
  • Organohalogen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Not Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
logPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP2.7ALOGPS
logP2.57ChemAxon
logS-1.5ALOGPS
pKa (Strongest Acidic)7.5ChemAxon
pKa (Strongest Basic)-6.9ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count2ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area40.46 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity39.63 m³·mol⁻¹ChemAxon
Polarizability14.95 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
Predicted GC-MS1,2-Benzenediol, 3,4-dichloro-, 1 TMS, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
Predicted GC-MS1,2-Benzenediol, 3,4-dichloro-, 1 TMS, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
Predicted GC-MS1,2-Benzenediol, 3,4-dichloro-, 2 TMS, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-0900000000-0fce000d3c17cad0305d2016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-004i-0900000000-3c49b4d02a9e0e0749b82016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-002f-2900000000-0e74dbdb3f1c9e5cbfc92016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-004i-0900000000-3fd566382f751290ff972016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-004i-0900000000-08de52f3896de67d6b752016-08-03View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0006-3900000000-85907268a054b9470cfa2016-08-03View Spectrum
NMRNot Available
Pathways
Pathways
Protein Targets
EnzymesNot Available
TransportersNot Available
Metal BindingsNot Available
ReceptorsNot Available
Transcriptional FactorsNot Available
Concentrations Data
Not Available
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound19877
PDB IDNot Available
ChEBI ID90882
References
General ReferencesNot Available