Weight | 100.117 g/mol |
---|---|
Formula | C5H8O2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
2-PENTENOIC ACID
626-98-2, 13991-37-2, 27516-53-6
Score:
#714 in Neuroscience
,
#1291 in Biochemistry
,
#3165 in Biology
,
#3961 in Chemistry
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- Synthesis and stereochemical assignment of trans-2-methyl-2-pentenoic acid and the corresponding esters, aldehydes, and alcohols (Journal of Organic Chemistry, 1968)
- Enantioselective hydrogenation of 2-methyl-2-pentenoic acid over cinchonidine-modified Pd / alumina (Catalysis Letters, 1996)
- Studies on the biotransformation in the perfused rat liver of 2-n-propyl-4-pentenoic acid, a metabolite of the antiepileptic drug valproic acid. Evidence for the formation of chemically reactive intermediates. (Drug Metabolism and Disposition, 1985)
- Metabolic activation of valproic acid and drug-mediated hepatotoxicity. Role of the terminal olefin, 2-n-propyl-4-pentenoic acid. (Chemical Research in Toxicology, 1988)
- Inhibition of medium-chain fatty acid -oxidationinvitro by valproic acid and its unsaturated metabolite, 2-n-propyl-4-pentenoic acid (Biochemical and Biophysical Research Communications, 1985)
- An efficient route to 1,3-amino hydroxyl system via electrophilic lactonization of 2-amino-4-pentenoic acid derivatives. Stereoselective synthesis of ()-bulgecinine (Tetrahedron Letters, 1986)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCC=CC(=O)O
-
InChIKeyYIYBQIKDCADOSF-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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