| Weight | 147.221 g/mol |
|---|---|
| Formula | C10H13N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
N-Cyclopropylbenzylamine (13324-66-8)
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- Effect of .alpha.-methylation on inactivation of monoamine oxidase by N-cyclopropylbenzylamine (Biochemistry, 1984)
- N-(1-Methyl)cyclopropylbenzylamine: a novel inactivator of mitochondrial monoamine oxidase. (Biochemical and Biophysical Research Communications, 1981)
- Revised mechanism for inactivation of mitochondrial monoamine oxidase by N-cyclopropylbenzylamine (Biochemistry, 1985)
- Mechanism for reactivation of N-cyclopropylbenzylamine-inactivated monoamine oxidase by amines. (Biochemistry, 1985)
- Syntheses of N-[1-2H]- and N-[1-3H]-cyclopropylbenzylamine and [phenyl-14C]-N-cyclopropylbenzylamine (Journal of Labelled Compounds and Radiopharmaceuticals, 1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC1NCC2=CC=CC=C2
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InChIKeyUSBAUXJPPHVCTF-UHFFFAOYSA-N
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Similar Compounds
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N-Cyclopropylbenzylamine
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