Metabolomics Structure Database

 
MW REGNO: 38332
Common Name:Cinnamaldehyde
Systematic Name:(2E)-3-phenylprop-2-enal
RefMet Name:Cinnamaldehyde
Synonyms: [PubChem Synonyms]
Exact Mass:
132.0575 (neutral)    Calculate m/z:
Formula:C9H8O
InChIKey:KJPRLNWUNMBNBZ-QPJJXVBHSA-N
ClassyFire superclass:Phenylpropanoids and polyketides [C0000261]
ClassyFire class:Cinnamaldehydes [C0000029]
ClassyFire subclass:Cinnamaldehydes [C0000029]
ClassyFire direct parent:Aromatic homomonocyclic compounds
MoNA MS spectra:View MS spectra
NP-MRD NMR spectra:View NMR spectra
SMILES:c1ccc(cc1)/C=C/C=O
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:637511
CHEBI ID:16731
HMDB ID:HMDB0003441
KEGG ID:C00903
Chemspider ID:553117
METLIN ID:6931
BMRB ID:bmse010257
MetaCyc ID:CINNAMALDEHYDE
NP-MRD ID(NMR):NP0000626
Plant Metabolite Hub(Pmhub):MS000006903

Calculated physicochemical properties (?):

Heavy Atoms: 10  
Rings: 1  
Aromatic Rings: 1  
Rotatable Bonds: 2  
van der Waals Molecular volume: 136.59 Å3 molecule-1  
Toplogical Polar Sufrace Area: 17.07 Å2 molecule-1  
Hydrogen Bond Donors: 0  
Hydrogen Bond Acceptors: 1  
logP: 1.90  
Molar Refractivity: 41.54  
Fraction sp3 Carbons: 0.00  
sp3 Carbons: 0  

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y

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