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341320 Sigma-Aldrich

Hydroquinine hydrobromide hydrate

98%

  • CAS Number 207386-86-5

  • Empirical Formula (Hill Notation) C20H26N2O2 · HBr · xH2O

  • Molecular Weight 407.34 (anhydrous basis)

  •  MDL number MFCD06656066

  •  PubChem Substance ID 329754839

  •  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   98%
optical activity   [α]25/D −100°, c = 1.9 in H2O
SMILES string   O.Br.CC[C@H]1CN2CC[C@H]1C[C@H]2[C@@H](O)c3ccnc4ccc(OC)cc34
InChI   1S/C20H26N2O2.BrH.H2O/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18;;/h4-6,8,11,13-14,19-20,23H,3,7,9-10,12H2,1-2H3;1H;1H2/t13-,14-,19-,20-;;/m0../s1
InChI key   IWSVSZYIGVGHCN-QTEGFKMESA-N

Description

Packaging

1 g in glass bottle

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Target organs 
Respiratory system
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable

Documents

Certificate of Analysis (COA)

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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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