
CAS 3399-73-3: 1-Cyclohexene-1-ethanamine
Formula:C8H15N
InChI:InChI=1S/C8H15N/c9-7-6-8-4-2-1-3-5-8/h4H,1-3,5-7,9H2
InChI key:InChIKey=IUDMXOOVKMKODN-UHFFFAOYSA-N
SMILES:C(CN)C=1CCCCC1
Synonyms:- 1-(2-Aminoethyl)cyclohexene
- 1-Cyclohexen-1-ylethylamine
- 1-Cyclohexene-1-ethanamine
- 1-Cyclohexene-1-ethylamine
- 2-(1-Cyclohexen-1-yl)ethylamine
- 2-(1-Cyclohexenyl)ethanamine
- 2-(1-Cyclolexenyl)Ethylamine
- 2-(Cyclohex-1-En-1-Yl)Ethanamine
- 2-(Cyclohex-1-en-1-yl)ethan-1-amine
- 2-Cyclohex-1-En-1-Ylethanaminium
- Cyclohex-1-ene-1-ethylamine
- See more synonyms
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Found 6 products.
2-(1-Cyclohexenyl)ethylamine
CAS:Formula:C8H15NPurity:>98.0%(GC)(T)Color and Shape:Colorless to Yellow clear liquidMolecular weight:125.222-(Cyclohex-1-en-1-yl)ethan-1-amine
CAS:2-(Cyclohex-1-en-1-yl)ethan-1-aminePurity:98%Molecular weight:125.21g/mol2-(Cyclohex-1-en-1-yl)ethanamine
CAS:Purity:95.0%Color and Shape:Liquid, ClearMolecular weight:125.214996337890622-(1-Cyclohexenyl)Ethylamine
CAS:Formula:C8H15NPurity:98%Color and Shape:LiquidMolecular weight:125.21142-(1-Cyclohexenyl)ethylamine
CAS:2-(1-Cyclohexenyl)ethylamine is an organic chemical that has a redox potential of 1.2 V, making it a strong reducing agent. It can be used as a catalyst in the hydrogen sulfate reduction method to generate ammonia from ammonium sulfate. 2-(1-Cyclohexenyl)ethylamine also reacts with amines to form substituted cyclohexenes and can be used in a reaction sequence for the synthesis of pyridine derivatives. 2-(1-Cyclohexenyl)ethylamine's molecular structure can be determined by NMR spectroscopy, which shows that this molecule is planar and has different vibrational modes. The optical properties of 2-(1-Cyclohexenyl)ethylamine are dependent on its environment and substituents.Formula:C8H15NPurity:Min. 95%Molecular weight:125.21 g/molRef: 3D-FC31603
Discontinued product2-(1-Cyclohexenyl)ethylamine
CAS:Controlled ProductFormula:C8H15NColor and Shape:NeatMolecular weight:125.21