| Weight | 116.12 g/mol |
|---|---|
| Formula | C4H8N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
SUCCINAMIDE (110-14-5)
Score:
#2703 in Biochemistry
,
#6695 in Chemistry
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- Poly(ethylenimine-co-L-lactamide-co-succinamide): A biodegradable polyethylenimine derivative with an advantageous pH dependent hydrolytic degradation for gene delivery (Bioconjugate Chemistry, 2002)
- Sequence-specific recognition of right-handed double-helical DNA by (2S,3S)- and (2R,3R)-dihydroxybis(netropsin)succinamide (Journal of the American Chemical Society, 1986)
- The stereoselective synthesis of succinamide derivatives via enolate oxidative coupling (Tetrahedron Letters, 1993)
- Synthesis of novel melanocortin 4 receptor agonists and antagonists containing a succinamide core (Bioorganic & Medicinal Chemistry Letters, 2004)
- A refinement of the crystal structure of succinamide (Acta Crystallographica, 1956)
- The dispersibility and stability of coal particles in hydrocarbon media with a polyisobutene succinamide dispersing agent (Colloids and Surfaces, 1984)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(CC(=O)N)C(=O)N
-
InChIKeySNCZNSNPXMPCGN-UHFFFAOYSA-N
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