| Weight | 119.076 g/mol |
|---|---|
| Formula | C3H5NO4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Methyl nitroacetate (2483-57-0)
nitroacetic acid methyl ester
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- Expedient synthesis of cyclopropane alpha-amino acids by the catalytic asymmetric cyclopropanation of alkenes using iodonium ylides derived from methyl nitroacetate. (Journal of the American Chemical Society, 2005)
- A NEW SYNTHESIS OF ALPHA -AMINO ACID DERIVATIVES EMPLOYING METHYL NITROACETATE AS A VERSATILE GLYCINE TEMPLATE (Journal of Organic Chemistry, 1998)
- Direct formation of C-glycofuranosyl derivatives by the reaction of d-aldoses with nitromethane and methyl nitroacetate (Carbohydrate Research, 1981)
- Carbon-carbon bond formation by means of substitution and addition reactions involving the polymer-supported carbanion from methyl nitroacetate (Tetrahedron Letters, 1984)
- Asymmetric addition of methyl nitroacetate to crotonaldehyde catalyzed by chiral amines (Russian Chemical Bulletin, 1993)
- Branched-chain sugars. Reaction of 1,2:5,6-di-O-isopropylidene--D-ribo-hexofuranos-3-ulose with sodium cyanide and methyl nitroacetate (Canadian Journal of Chemistry, 1976)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - nitroacetic acid methyl ester
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SMILESCOC(=O)C[N+](=O)[O-]
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InChIKeyALBSWLMUHHZLLR-UHFFFAOYSA-N
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