Weight | 99.089 g/mol |
---|---|
Formula | C4H5NO2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
METHYL CYANOACETATE (105-34-0)
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- Calcite and fluorite as catalyst for the Knvenagel condensation of malononitrile and methyl cyanoacetate under solvent-free conditions (Tetrahedron Letters, 2003)
- Missing conformers. Comparative study of conformational cooling in cyanoacetic acid and methyl cyanoacetate isolated in low temperature inert gas matrixes (Chemical Physics Letters, 2003)
- Synthesis of 5cyanopyrazolo[3,4b]pyridines in the reaction of 5amino3methyl1phenylpyrazole with arylidene derivatives of malonodinitrile and ethyl cyanoacetate (Journal of Heterocyclic Chemistry, 1999)
- Ion Pair Extraction in Preparative Organic Chemistry. III. Alkylation of Methyl Cyanoacetate and Related Compounds. (Acta Chemica Scandinavica, 1969)
- Conformational isomerism in methyl cyanoacetate: A combined matrix-isolation infrared spectroscopy and molecular orbital study (Physical Chemistry Chemical Physics, 2001)
- Construction of 1,2,5Tricarbonyl Compounds using Methyl Cyanoacetate as a Glyoxylate Anion Synthon Combined with Copper(I) IodideCatalyzed Aerobic Oxidation (Advanced Synthesis & Catalysis, 2011)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC(=O)CC#N
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