Showing Compound Card for 1,2-dimethyl-1H-Indole (CDB005809)

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Record Information
Version1.0
Created at2020-04-27 16:58:43 UTC
Updated at2021-01-04 18:49:22 UTC
CannabisDB IDCDB005809
Secondary Accession NumbersNot Available
Cannabis Compound Identification
Common Name1,2-dimethyl-1H-Indole
Description1,2-Dimethylindole also known as 1,2-dimethyl-1H-Indole is a dimethylated derivative of indole in which two methyl substituents positioning on N-1 and C-3 of indole. 1,2-Dimethylindole belongs to the class of organic compounds known as N-alkylindoles. N-alkylindoles are compounds containing an indole moiety that carries an alkyl chain at the 1-position. 1,2-Dimethylindole is one of several structural isomers of dimethylindole wherein two methyl groups are substituted by two methyl groups at different positions of indole. 1,2-Dimethylindole is widely used as an intermediate in chemical synthesis to prepare herbicides and various pharmaceuticals. Dimethylindoles are found in cannabis smoke. 1,2-Dimethylindole is formed during the combustion of cannabis ( Ref:DOI ).
Structure
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MOLSDF3D-SDFPDBSMILESInChI View 3D Structure
SynonymsNot Available
Chemical FormulaC10H11N
Average Molecular Weight145.21
Monoisotopic Molecular Weight145.0891
IUPAC Name1,2-dimethyl-1H-indole
Traditional Name1,2-dimethylindole
CAS Registry Number875-79-6
SMILES
CN1C(C)=CC2=CC=CC=C12
InChI Identifier
InChI=1S/C10H11N/c1-8-7-9-5-3-4-6-10(9)11(8)2/h3-7H,1-2H3
InChI KeyBJMUOUXGBFNLSN-UHFFFAOYSA-N
Chemical Taxonomy
ClassificationNot classified
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
logP2.97ALOGPS
logP2.5ChemAxon
logS-2.4ALOGPS
Physiological Charge0ChemAxon
Hydrogen Acceptor Count0ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area4.93 ŲChemAxon
Rotatable Bond Count0ChemAxon
Refractivity47.19 m³·mol⁻¹ChemAxon
Polarizability17.13 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Spectra
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 ID12834
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound13408
PDB IDNot Available
ChEBI IDNot Available
References
General ReferencesNot Available