| Weight | 100.117 g/mol |
|---|---|
| Formula | C5H8O2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
TIGLIC ACID (13201-46-2, 80-59-1)
tiglic acid, (Z)-isomer · tiglic acid, (E)-isomer · trans-2-methylcrotonic acid
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- A two-dimensional NMR study of angelic and tiglic acid (Magnetic Resonance in Chemistry, 1984)
- Asymmetric synthesis by chiral ruthenium complexes: XI. Asymmetric hydrogenation of tiglic acid in the presence of phosphine substituted ruthenium carbonyl carboxylates (Journal of Organometallic Chemistry, 1985)
- Condensation of crotonic and tiglic acid dianions with aldehydes and ketones (Journal of Organic Chemistry, 1984)
- Regioselective Synthesis of 2-Hydroperoxy-2-methylenebutanoic Acid Derivatives via Photooxygenation of Tiglic Acid Derivatives (Synthesis, 1986)
- Single-crystal-to-single-crystal E ! Z isomerization of tiglic acid in a supramolecular framework (Acta Crystallographica Section B-structural Science, 2007)
- Efficient -facial control in the ene reaction of nitrosoarene, triazolinedione, and singlet oxygen with tiglic amides of the bornane-derived sultam as chiral auxiliary: An economical synthesis of enantiomerically pure nitrogen- and oxygen-functionalized acrylic acid derivatives (Journal of the American Chemical Society, 2002)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - tiglic acid, (Z)-isomer
- tiglic acid, (E)-isomer
- trans-2-methylcrotonic acid
-
SMILESCC=C(C)C(=O)O
-
InChIKeyUIERETOOQGIECD-UHFFFAOYSA-N
- Pubchem - TIGLIC ACID
- Wikipedia - (E)-2,3-dimethylacrylic acid
Tiglic acid is a monocarboxylic unsaturated organic acid. It is found in croton oil and in several other natural products. It was also isolated from the defensive secretion of certain beetles.
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1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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TIGLIC ACID
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