Record Information
Version1.0
Creation date2010-04-08 22:14:42 UTC
Update date2015-07-21 06:40:38 UTC
Primary IDFDB019946
Secondary Accession NumbersNot Available
Chemical Information
FooDB Name1-(5-Methyl-2-thienyl)-1-propanone
Description1-(5-Methyl-2-thienyl)-1-propanone belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group. Based on a literature review very few articles have been published on 1-(5-Methyl-2-thienyl)-1-propanone.
CAS Number59303-13-8
Structure
Thumb
Synonyms
Predicted Properties
PropertyValueSource
Water Solubility0.47 g/LALOGPS
logP2.23ALOGPS
logP2.79ChemAxon
logS-2.5ALOGPS
pKa (Strongest Acidic)15.75ChemAxon
pKa (Strongest Basic)-7.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area17.07 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity43.03 m³·mol⁻¹ChemAxon
Polarizability17.04 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleNoChemAxon
Chemical FormulaC8H10OS
IUPAC name1-(5-methylthiophen-2-yl)propan-1-one
InChI IdentifierInChI=1S/C8H10OS/c1-3-7(9)8-5-4-6(2)10-8/h4-5H,3H2,1-2H3
InChI KeyROPOMQPSWIOWSN-UHFFFAOYSA-N
Isomeric SMILESCCC(=O)C1=CC=C(C)S1
Average Molecular Weight154.229
Monoisotopic Molecular Weight154.045235632
Classification
Description Belongs to the class of organic compounds known as aryl alkyl ketones. These are ketones have the generic structure RC(=O)R', where R = aryl group and R'=alkyl group.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbonyl compounds
Direct ParentAryl alkyl ketones
Alternative Parents
Substituents
  • Aryl alkyl ketone
  • 2,5-disubstituted thiophene
  • Heteroaromatic compound
  • Thiophene
  • Organoheterocyclic compound
  • Organic oxide
  • Hydrocarbon derivative
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Source:

Biological location:

Role

Industrial application:

Biological role:

Physico-Chemical Properties
Physico-Chemical Properties - Experimental
Spectra
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
GC-MS1-(5-Methyl-2-thienyl)-1-propanone, non-derivatized, GC-MS Spectrumsplash10-0fb9-4900000000-b9ecb96d90cba0c1ee5aSpectrum
GC-MS1-(5-Methyl-2-thienyl)-1-propanone, non-derivatized, GC-MS Spectrumsplash10-0fb9-4900000000-b9ecb96d90cba0c1ee5aSpectrum
Predicted GC-MS1-(5-Methyl-2-thienyl)-1-propanone, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positivesplash10-0fb9-9400000000-57f3400d76df1a9b24c7Spectrum
Predicted GC-MS1-(5-Methyl-2-thienyl)-1-propanone, non-derivatized, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0a4i-0900000000-5e85a4b649949e77cb432017-09-01View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-9700000000-633aaa3c9d4f58f447d42017-09-01View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0f6t-9200000000-3275d39c655fcd045c292017-09-01View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-0900000000-d591ee9cc637ffe5ba3d2017-09-01View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0udj-8900000000-8f3175f9856940bc6b182017-09-01View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-08gj-9100000000-b9f86e22c86a7da335a22017-09-01View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udj-4900000000-3da24068d89ae3a61b432021-09-23View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0002-9000000000-0c13be151c8b7edd48a92021-09-23View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0002-9000000000-aa2f532a8f6b029108d92021-09-23View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0a4i-1900000000-98661aa9978319abc2062021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-9100000000-292711eada1c62abb3ba2021-09-24View Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01ot-9100000000-b38906c710098e07e6bc2021-09-24View Spectrum
NMRNot Available
ChemSpider ID504500
ChEMBL IDNot Available
KEGG Compound IDNot Available
Pubchem Compound ID580407
Pubchem Substance IDNot Available
ChEBI IDNot Available
Phenol-Explorer IDNot Available
DrugBank IDNot Available
HMDB IDHMDB40231
CRC / DFC (Dictionary of Food Compounds) IDMGY43-U:MGY43-U
EAFUS IDNot Available
Dr. Duke IDNot Available
BIGG IDNot Available
KNApSAcK IDNot Available
HET IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
Flavornet IDNot Available
GoodScent IDNot Available
SuperScent IDNot Available
Wikipedia IDNot Available
Phenol-Explorer Metabolite IDNot Available
Duplicate IDSNot Available
Old DFC IDSNot Available
Associated Foods
FoodContent Range AverageReference
Processing...
Biological Effects and Interactions
Health Effects / BioactivitiesNot Available
EnzymesNot Available
PathwaysNot Available
MetabolismNot Available
BiosynthesisNot Available
Organoleptic Properties
FlavoursNot Available
Files
MSDSNot Available
References
Synthesis ReferenceNot Available
General ReferenceNot Available
Content Reference