9-Amino-(9-deoxy)epi-quinine trihydrochloride
9-Amino-(9-deoxy)epi-quinine trihydrochloride Basic information
- Product Name:
- 9-Amino-(9-deoxy)epi-quinine trihydrochloride
- Synonyms:
-
- (8α,9S)-6′-Methoxycinchonan-9-amine trihydrochloride
- (8alpha,9S)-6'-Methoxycinchonan-9-amine trihydrochloride >=90%
- (S)-{5-Ethenyl-1-azabicyclo[2.2.2]octan-2-yl}-(6-methoxyquinolin-4-yl)methanamine trihydrochlo
- (8Α,9S)-6'-METHOXYCINCHONAN-9-AMINETRIHYDROCHLORIDE,MIN.90%
- (8α, 9S)-6'-Methoxycinchonan-9-amine trihydrochloride, min. 90%
- (S)-(5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl)-(6-methoxyquinolin-4-yl)methanamine:trihydrochloride
- 9S)-6'-Methoxycinchonan-9-amine trihydrochloride, min. 90%
- (8ALPHA,9S)-6-METHOXYCINCHONAN-9-AMINE TRIHYDROCHLORIDE
- CAS:
- 1231763-32-8
- MF:
- C20H28Cl3N3O
- MW:
- 432.81482
- Mol File:
- 1231763-32-8.mol
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9-Amino-(9-deoxy)epi-quinine trihydrochloride Chemical Properties
- alpha
- +59.4° (c=1.0, H2O)
- form
- Powder
- color
- pale yellow
- optical activity
- [α]/D +65.0±2.0°, c = 1 in 0.1 M HCl
- Stability:
- store cold
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9-Amino-(9-deoxy)epi-quinine trihydrochloride Usage And Synthesis
Reaction
- Aza-Michael reactions on α,β-unsaturated ketones.
- Epoxidation of α,β-unsaturated ketones.
- Epoxidation of α,β-unsaturated aldehydes.
- Nitrocyclopropanation of α,β-unsaturated ketones.
- Diels-Alder reaction.
- Intramolecular aldolization of diketones.
- Friedel-Crafts alkylation of indoles with α,β-unsaturated ketones.
- Friedel-Crafts/amination cascade reactions with a-substituted α,β-unsaturated aldehydes.
- Aziridination of acyclic α,β-unsaturated ketones.
- Aziridination of cyclic α,β-unsaturated ketones.
- Double Michael cascade process.
- α-fluorination of cyclic ketones.
Chemical Properties
Solid
9-Amino-(9-deoxy)epi-quinine trihydrochlorideSupplier
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