| Weight | 87.166 g/mol |
|---|---|
| Formula | C5H13N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
2-AMINOPENTANE
63493-28-7, 625-30-9, 41444-43-3
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- A Multidisciplinary Approach Toward the Rapid and Preparative-Scale Biocatalytic Synthesis of Chiral Amino Alcohols: A Concise Transketolase-/omega-Transaminase-Mediated Synthesis of (2S,3S)-2-Aminopentane-1,3-diol (Organic Process Research & Development, 2010)
- Catalyst-controlled reversal of chemoselectivity in acylation of 2-aminopentane-1,5-diol derivatives (Chemical Communications, 2012)
- 1-(Benzofuran-2-yl)-2-(3,3,3-trifluoropropyl)aminopentane HCl, 3-F-BPAP, antagonizes the enhancer effect of (-)-BPAP in the shuttle box and leaves the effect of (-)-deprenyl unchanged (Life Sciences, 2002)
- 2-propyl-1-aminopentane, its deamination by monoamine oxidase and semicarbazide-sensitive amine oxidase, conversion to valproic acid and behavioral effects (Neuropharmacology, 1991)
- Some pharmacological implications of MAO-mediated deamination of branched aliphatic amines: 2-Propyl-1-aminopentane and N-(2-propylpentyl)glycinamide as valproic acid precursors (Journal of Neural Transmission-supplement, 1990)
- Deamination of 2-propyl-1-aminopentane and 2-[(2-propyl)pentylamino] acetamide by amine oxidases: formation of valproic acid. (Progress in Neuro-psychopharmacology & Biological Psychiatry, 1991)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCC(C)N
-
InChIKeyIGEIPFLJVCPEKU-UHFFFAOYSA-N
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