Weight | 154.121 g/mol |
---|---|
Formula | C7H6O4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Methyl coumalate (6018-41-3)
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- First inverse electron-demand Diels-Alder methodology of 3-chloroindoles and methyl coumalate to carbazoles. (Organic Letters, 2014)
- Diels-Alder reaction of methyl coumalate with 1,3-dienes (Tetrahedron, 1974)
- Et3N-Catalyzed Tandem Formal [4 + 3] Annulation/Decarboxylation/Isomerization of Methyl Coumalate with Imine Esters: Access to Functionalized Azepine Derivatives (Organic Letters, 2014)
- Aromatics from pyrones: para-substituted alkyl benzoates from alkenes, coumalic acid and methyl coumalate (Green Chemistry, 2011)
- One-pot formal synthesis of biorenewable terephthalic acid from methyl coumalate and methyl pyruvate (Green Chemistry, 2014)
- Divergent DielsAlder methodology from methyl coumalate toward functionalized aromatics (Tetrahedron Letters, 2013)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)C1=COC(=O)C=C1
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InChIKeyHHWWWZQYHPFCBY-UHFFFAOYSA-N
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