| Weight | 141.17 g/mol |
|---|---|
| Formula | C7H11NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
tert-Butyl cyanoacetate (1116-98-9)
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- A colorimetric probe based on diketopyrrolopyrrole and tert-butyl cyanoacetate for cyanide detection (New Journal of Chemistry, 2015)
- Iridium catalysed alkylation of tert-butyl cyanoacetate with alcohols under solvent free conditions (Tetrahedron, 2009)
- X-Ray Crystal Structures of the Enolate of tert-Butyl -Cyanoacetate with Li+ or Protonated 1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU-H+) as Gegenion. NH Hydrogen Bridge from DBU-H+ to the Enolate Oxygen Atom (Chemische Berichte, 1994)
- Reaction of 3-hetero-1,5-dialdehydes with tert-butyl cyanoacetate (Carbohydrate Research, 1986)
- Palladium-Catalyzed Carbonylative -Arylation of tert-Butyl Cyanoacetate with (Hetero)aryl Bromides. (Journal of Organic Chemistry, 2016)
- Chemistry of iminofurans: XIII. Recyclization of 4-arylamino-2-tert-butyl-5-oxo-2,5-dihydrofuran-2-yl acetates with ethyl cyanoacetate (Russian Journal of Organic Chemistry, 2016)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)OC(=O)CC#N
-
InChIKeyBFNYNEMRWHFIMR-UHFFFAOYSA-N
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tert-Butyl cyanoacetate
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