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420328 Sigma-Aldrich

Cinchonine monohydrochloride hydrate

99%

Synonym: Cinchonan-9(S)-ol monohydrochloride

  • CAS Number 206986-88-1

  • Empirical Formula (Hill Notation) C19H22N2O · HCl · xH2O

  • Molecular Weight 330.85 (anhydrous basis)

  •  Beilstein/REAXYS Number 5784953

  •  MDL number MFCD00191936

  •  PubChem Substance ID 24866328

  •  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   200
assay   99%
optical activity   [α]20/D +101°, c = 1 in chloroform
mp   208-218 °C (lit.)
SMILES string   O[C@H]([C@H]1CC2CCN1C[C@@H]2C=C)c3ccnc4ccccc34
InChI   1S/C19H22N2O/c1-2-13-12-21-10-8-14(13)11-18(21)19(22)16-7-9-20-17-6-4-3-5-15(16)17/h2-7,9,13-14,18-19,22H,1,8,10-12H2/t13-,14?,18+,19-/m0/s1
InChI key   KMPWYEUPVWOPIM-FGVBSWQGSA-N

Description

Packaging

50 mg in glass bottle

Bottomless glass bottle. Contents are inside inserted fused cone.

Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
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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