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07317 Sigma-Aldrich

(2S,4S,5R)-2-Aminomethyl-5-ethylquinuclidine

≥95.0% (GC)

Synonym: (2S,4S,5R)-5-Ethyl-2-quinuclidinyl-methylamine

  • CAS Number 475160-59-9

  • Empirical Formula (Hill Notation) C10H20N2

  • Molecular Weight 168.28

  •  PubChem Substance ID 24846048

  •  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   ≥95.0% (GC)
storage temp.   2-8°C
SMILES string   CC[C@H]1CN2CCC1C[C@H]2CN

Description

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Analysis Note

diastereometric excess 98% (against (2R,4S,5R)-2-Aminomethyl-5-ethylquinuclidine)

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
NONH for all modes of transport
WGK Germany 
3

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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