| Weight | 101.149 g/mol |
|---|---|
| Formula | C5H11NO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Pentanamide (626-97-1)
valeramide
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- Dissociation behavior of ionized valeramide: Part I. Experimental studies (International Journal of Mass Spectrometry, 2002)
- ABSOLUTE CONFIGURATION OF THE FOUR STEREOISOMERS OF VALNOCTAMIDE (2-ETHYL-3-METHYL VALERAMIDE), A POTENTIALLY NEW STEREOSPECIFIC ANTIEPILEPTIC AND CNS DRUG (Tetrahedron-asymmetry, 1999)
- Dissociation behavior of ionized valeramide: Part II. Theoretical exploration of the potential-energy surface (International Journal of Mass Spectrometry, 2002)
- Dissociation behavior of ionized valeramide: Part III. An unprecedented temperature effect on the C3/C2 branching ratio and its implications for metastable ion dissociations (International Journal of Mass Spectrometry, 2002)
- Regio- and diastereoselective CH bond activation of valeramide and 3-methyl valeramide by bare Fe+ ions (International Journal of Mass Spectrometry, 2002)
- Diastereoselectivity in the McLafferty rearrangement of photoionized 3-methyl valeramide (Journal of Organic Chemistry, 2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - valeramide
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SMILESCCCCC(=O)N
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InChIKeyIPWFJLQDVFKJDU-UHFFFAOYSA-N
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