| Weight | 57.096 g/mol |
|---|---|
| Formula | C3H7N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Cyclopropylamine (765-30-0)
cyclopropylamine hydrochloride · cyclopropylamine acetate · cyclopropylamine, 3H-labeled
Score:
#1903 in Physics
,
#5956 in Chemistry
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- Kinetic studies and effects in vivo of a new monoamine oxidase inhibitor, N[2(ochlorophenoxy)-ethyl]-cyclopropylamine (Biochemical Pharmacology, 1968)
- Formation of cyclopropanone during cytochrome P450-catalyzed N-dealkylation of a cyclopropylamine. (Journal of the American Chemical Society, 2002)
- The molecular structures of methylcyclopropane, cyclopropylamine and cyclopropyl lithium (Journal of Molecular Structure, 1978)
- Highly Enantioselective Synthesis of Cyclopropylamine Derivatives via Ru(II)-Pheox-Catalyzed Direct Asymmetric Cyclopropanation of Vinylcarbamates (Organic Letters, 2013)
- N-dealkylation of an N-cyclopropylamine by horseradish peroxidase. Fate of the cyclopropyl group. (Journal of the American Chemical Society, 2001)
- Synthesis, Biological Activity and Mechanistic Insights of 1-Substituted Cyclopropylamine Derivatives: A Novel Class of Irreversible Inhibitors of Histone Demethylase Kdm1A. (European Journal of Medicinal Chemistry, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cyclopropylamine hydrochloride
- cyclopropylamine acetate
- cyclopropylamine, 3H-labeled
-
SMILESC1CC1N
-
InChIKeyHTJDQJBWANPRPF-UHFFFAOYSA-N
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