| Weight | 162.403 g/mol |
|---|---|
| Formula | C2H2Cl3NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2,2,2-Trichloroacetamide (594-65-0)
trichloroacetimidate · trichloroacetamide
Score:
#1906 in Physics
,
#2381 in Biochemistry
,
#5970 in Chemistry
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- Anomeric-Oxygen Activation for Glycoside Synthesis: The Trichloroacetimidate Method (Advances in Carbohydrate Chemistry and Biochemistry, 1994)
- O-(-D-Glucopyranosyl)trichloroacetimidate as a Glucosyl Donor (Journal of Carbohydrate Chemistry, 1985)
- Synthesis of tigogenyl -O-cellobioside heptaacetate and glycoside tetraacetate via Schmidt's trichloroacetimidate method; some new observatons. (Tetrahedron Letters, 1990)
- Direct o-glycosyl trichloroacetimidate formation, nucleophilicity of the anomeric oxygen atom (Tetrahedron Letters, 1984)
- Kinetic and Computational Analysis of the Palladium(II)-Catalyzed Asymmetric Allylic Trichloroacetimidate Rearrangement: Development of a Model for Enantioselectivity (Journal of the American Chemical Society, 2007)
- The Application of the Trichloroacetimidate Method to the Synthesis of -D-Gluco- and -D-Galactopyranosides (Journal of Carbohydrate Chemistry, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - trichloroacetimidate
- trichloroacetamide
-
SMILESC(=O)(C(Cl)(Cl)Cl)N
-
InChIKeyUPQQXPKAYZYUKO-UHFFFAOYSA-N
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