| Weight | 127.231 g/mol |
|---|---|
| Formula | C8H17N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1-Cyclohexylethylamine (4352-49-2)
54423-01-7 · (1-cyclohexylethyl)amine
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- Enantiomeric separation of 1-phenylethylamine and 1-cyclohexylethylamine in capillary electrophoresis with contactless conductivity detection (Journal of Chromatography A, 2005)
- Resolution of 1-cyclohexylethylamine via diastereomeric salt formation with enantiopure 2-phenylacetic acids (Tetrahedron-asymmetry, 2006)
- Molecular mechanism of DCR phenomenon observed in (RS)-1-cyclohexylethylamine-mandelic acid resolution system (Tetrahedron-asymmetry, 2006)
- Synthesis of Optically Active Polyamines Based on Chiral 1-Cyclohexylethylamine Derivatives (Polymer Journal, 2009)
- Functionalization of Keggin type manganese substituted phosphotungstate by R-()-1-cyclohexylethylamine: Synthesis and characterization (Inorganica Chimica Acta, 2012)
- Preparation of the chiral amine salts [(5-C5H5)Ru(PPh3)(CNtBu)(NH2R)]PF6, RNH2 = -methylbenzylamine, 1-cyclohexylethylamine, and 1-(1-naphthyl)ethylamine: X-ray single crystal structures of the diastereomeric salts (SRuRC)- and (RRuRC)-[(5-C5H5)Ru(PPh3)(CNtBu){NH2CH(Me)(Ph)}]PF6 (Polyhedron, 2006)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 54423-01-7
- (1-cyclohexylethyl)amine
-
SMILESCC(C1CCCCC1)N
-
InChIKeyXBWOPGDJMAJJDG-UHFFFAOYSA-N
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