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381950 Sigma-Aldrich

Hydroquinidine 9-phenanthryl ether

96%

Synonym: O-(9-Phenanthryl)hydroquinidine

  • CAS Number 135042-88-5

  • Empirical Formula (Hill Notation) C34H34N2O2

  • Molecular Weight 502.65

  •  Beilstein/REAXYS Number 4848701

  •  MDL number MFCD00134564

  •  PubChem Substance ID 24863851

  •  NACRES NA.22

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Cinchona Alkaloids, Privileged Ligands and Complexes More...
Quality Level   100
assay   96%
optical activity   [α]20/D −348°, c = 1 in ethanol
mp   112 °C (dec.) (lit.)
SMILES string   CC[C@@H]1CN2CC[C@H]1C[C@@H]2[C@@H](Oc3cc4ccccc4c5ccccc35)c6ccnc7ccc(OC)cc67
InChI   1S/C34H34N2O2/c1-3-22-21-36-17-15-23(22)18-32(36)34(29-14-16-35-31-13-12-25(37-2)20-30(29)31)38-33-19-24-8-4-5-9-26(24)27-10-6-7-11-28(27)33/h4-14,16,19-20,22-23,32,34H,3,15,17-18,21H2,1-2H3/t22-,23+,32-,34+/m1/s1
InChI key   TWOVHUYOMTVDRB-FVSKFNOUSA-N

Description

Packaging

1 g in glass bottle

Legal Information

Sold under license from Rhodia Pharma Solutions.

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable
Protocols & Articles

Articles

Cinchona Alkaloids - Aldrich ChemFiles 2008, 8.2, 74.

Cinchona alkaloids and their derivatives have proven to catalyze an astonishing array of enantioselective transformations, providing access to chiral products of high enantiopurity.1 The presence of ...
William Sommer and Daniel Weibel
Aldrich ChemFiles 2008, 8.2, 74.
Keywords: Addition reactions, Aminations, Antimicrobials, Asymmetric synthesis, Catalysis, Desymmetrizations, Dihydroxylations, Ligands, Reductive aminations

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