| Weight | 113.116 g/mol |
|---|---|
| Formula | C5H7NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Ethyl isocyanoacetate (2999-46-4)
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- Synthesis and X-ray Crystal Structures of Palladium(II) and Platinum(II) Complexes of the PCP-Type Chiral Tridentate Ligand (1R,1'R)-1,3-Bis(1-(diphenylphosphino)ethyl)benzene. Use in the Asymmetric Aldol Reaction of Methyl Isocyanoacetate and Aldehydes (Organometallics, 1998)
- Tandem Double-Michael-Addition/Cyclization/Acyl Migration of 1,4-Dien-3-ones and Ethyl Isocyanoacetate : Stereoselective Synthesis of Pyrrolizidines (Angewandte Chemie, 2009)
- Ethyl 2Oxazoline5carboxylate from Ethyl Isocyanoacetate and Carbonyl Compounds (Angewandte Chemie, 1970)
- Dipolar Cycloaddition of Ethyl Isocyanoacetate to 3-Chloro-2-(methylthio)/2-(methylsulfonyl)quinoxalines: Highly Regio- and Chemoselective Synthesis of Substituted Imidazo[1,5-a]quinoxaline-3-carboxylates. (Journal of Organic Chemistry, 2007)
- Ethyl Isocyanoacetate as a Useful Glycine Equivalent (Synlett, 2010)
- Synthesis of conformationally constrained -amino acid derivatives using ethyl isocyanoacetate as glycine equivalent (Bioorganic & Medicinal Chemistry Letters, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)C[N+]#[C-]
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InChIKeyFPULFENIJDPZBX-UHFFFAOYSA-N
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