| Weight | 86.09 g/mol |
|---|---|
| Formula | C4H6O2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Isocrotonic acid (3724-65-0, 503-64-0)
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- Favorsky Rearrangements. I. A New Synthesis of Isocrotonic Acid. (Acta Chemica Scandinavica, 1963)
- OXIDATION OF UNSATURATED COMPOUNDS. I. OXIDATION OF CROTONIC AND ISOCROTONIC ACIDS, OF THE LACTONE OF 3-HYDROXY-ISOCROTONIC ACID AND OF MALEIC ANHYDRIDE (Journal of the American Chemical Society, 1929)
- Effect of chloro- and bromo-derivatives of isocrotonic acid of bioenergetic processes in Ehrlich ascites cells and isolated mitochondria. (Neoplasma, 1979)
- Studies in decarboxylation. Part 14. The gas-phase decarboxylation of but-3-enoic acid and the intermediacy of isocrotonic (cis-but-2-enoic) acid in its isomerisation to crotonic (trans-but-2-enoic) acid (Journal of The Chemical Society-perkin Transactions 1, 1982)
- Reactivities of Crotonic Acid and Isocrotonic Acid in Radical Copolymerizations (Journal of Synthetic Organic Chemistry Japan, 1969)
- Characteristics of the toxic effect and safety level of water pollution by crotonic and isocrotonic acid nitriles (Gigiena i sanitariia, 1972)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC=CC(=O)O
-
InChIKeyLDHQCZJRKDOVOX-UHFFFAOYSA-N
- Pubchem - Isocrotonic acid
- Wikipedia - isocrotonic acid
Isocrotonic acid (or quartenylic acid) is the cis analogue of crotonic acid. It is an oil, possessing a smell similar to that of brown sugar. It boils at 171.9C, concomitant with conversion into crotonic acid.
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Isocrotonic acid
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