| Identification | Back Directory | [Name]
HYDROQUINIDINE 9-PHENANTHRYL ETHER | [CAS]
135042-88-5 | [Synonyms]
o-(9-phenanthryl)hydroquinidine
(9S)-10,11-dihydro-6'-Methoxy-9-(9-phenanthrenyloxy)-Cinchonan
Cinchonan, 10,11-dihydro-6'-Methoxy-9-(9-phenanthrenyloxy)-, (9S)-
(1S,2R,4S,5R)-5-Ethyl-2-((S)-(6-methoxyquinolin-4-yl)(phenanthren-9-yloxy)methyl)quinuclidine
4-[(S)-[(2R,4S,5S)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-phenanthren-9-yloxymethyl]-6-methoxyquinoline | [Molecular Formula]
C34H34N2O2 | [MDL Number]
MFCD32856213 | [MOL File]
135042-88-5.mol | [Molecular Weight]
502.65 |
| Chemical Properties | Back Directory | [Melting point ]
112 °C (dec.)(lit.) | [Boiling point ]
690.3±40.0 °C(Predicted) | [density ]
1.24±0.1 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
9?+-.0.70(Predicted) | [optical activity]
[α]20/D 348°, c = 1 in ethanol | [BRN ]
4848701 |
| Hazard Information | Back Directory | [Uses]
Hydroquinidine 9-Phenanthryl Ether acts as a reagent for the synthesis of antifugal indole alkaloids and N-reverse prenylated tryptophan. Also, acts as a reagent for the synthesis of deoxy sugar via Wharton rearrangement and stereoselective dihydroxylation reaction. |
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