| Weight | 114.148 g/mol |
|---|---|
| Formula | C5H10N2O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
L-prolinamide (7531-52-4)
prolinamide · prolinamide, (L)-isomer · 2-pyrrolidinecarboxamide
Score:
#6218 in Chemistry
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- Prolactin and thyrotropin release in man by synthetic pyroglutamyl-histidyl-prolinamide (Biochemical and Biophysical Research Communications, 1971)
- Enantioselective direct aldol reactions catalyzed by l-prolinamide derivatives (Proceedings of the National Academy of Sciences of the United States of America, 2004)
- Catalysts for the Asymmetric Transfer Hydrogenation of Ketones Derived from l-Prolinamide and (p-CymeneRuCl2)2 or (Cp*RhCl2)2 (Organometallics, 2001)
- Polystyrene-Supported Proline and Prolinamide. Versatile Heterogeneous Organocatalysts Both for Asymmetric Aldol Reaction in Water and -Selenenylation of Aldehydes. (Tetrahedron Letters, 2007)
- Chemically L-prolinamide-modified monolithic silica column for enantiomeric separation of dansyl amino acids and hydroxy acids by capillary electrochromatography and -high performance liquid chromatography (Electrophoresis, 2001)
- Direct Asymmetric Aldol Reaction Catalyzed by Simple Prolinamide Phenols. (Tetrahedron-asymmetry, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - prolinamide
- prolinamide, (L)-isomer
- 2-pyrrolidinecarboxamide
-
SMILESC1CC(NC1)C(=O)N
-
InChIKeyVLJNHYLEOZPXFW-UHFFFAOYSA-N
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L-prolinamide
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