Metabolomics Structure Database

 
MW REGNO: 41876
Common Name:3-Methyl-2-butenal
Systematic Name:3-methylbut-2-enal
RefMet Name:3-Methyl-2-butenal
Synonyms: [PubChem Synonyms]
Exact Mass:
84.0575 (neutral)    Calculate m/z:
Formula:C5H8O
InChIKey:SEPQTYODOKLVSB-UHFFFAOYSA-N
ClassyFire superclass:Organic oxygen compounds
ClassyFire class:Organooxygen compounds
ClassyFire subclass:Carbonyl compounds
ClassyFire direct parent:Enals
Massbank MS spectra:View MS spectra
SMILES:CC(=CC=O)C
Studies:Available studies (via RefMet name)

Select appropriate tab below to view additional details:

External database links:

PubChem CID:61020
CHEBI ID:15825
HMDB ID:HMDB0012157
KEGG ID:C07330
Chemspider ID:54980
BMRB ID:bmse000474
MetaCyc ID:PRENAL
Plant Metabolite Hub(Pmhub):MS000015923

Calculated physicochemical properties (?):

Heavy Atoms: 6  
Rings: 0  
Aromatic Rings: 0  
Rotatable Bonds: 1  
van der Waals Molecular volume: 98.57 Å3 molecule-1  
Toplogical Polar Sufrace Area: 17.07 Å2 molecule-1  
Hydrogen Bond Donors: 0  
Hydrogen Bond Acceptors: 1  
logP: 1.15  
Molar Refractivity: 25.50  
Fraction sp3 Carbons: 0.40  
sp3 Carbons: 2  

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
NPClassifier classification: "NPClassifier: A Deep Neural Network-Based Structural Classification Tool for Natural Products", Kim HW, Wang M, Leber CA, Nothias LF, Reher R, Kang KB, van der Hooft JJJ, Dorrestein PC, Gerwick WH and Cottrell GW. J Nat Prod. 2021 Nov 26;84(11):2795-2807.DOI: 10.1021/acs.jnatprod.1c00399.

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