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  • 669172 - (S)-(+)-3,3′-Bis(3,5-dimethylphenyl)-5,5′,6,6′,7,7′,8,8′-octahydro-1,1′-bi-2-naphthol

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669172 Aldrich

(S)-(+)-3,3′-Bis(3,5-dimethylphenyl)-5,5′,6,6′,7,7′,8,8′-octahydro-1,1′-bi-2-naphthol

97%

Synonym: (S)-3,3′-bis(3,5-dimethylphenyl)-5,6,7,8,5′,6′,7′,8′-octahydro-[1,1′]binaphthalenyl-2,2′-diol

  • Empirical Formula (Hill Notation) C36H38O2

  • Molecular Weight 502.69

  •  MDL number MFCD08457658

  •  PubChem Substance ID 24885024

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Properties

Related Categories Asymmetric Synthesis, BINOLs, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Other Organocatalysts,
InChI Key   RSHMDLJRFPHHRE-UHFFFAOYSA-N
assay   97%
mp   218-222 °C

Description

Packaging

100 mg in glass insert

Price and Availability

Safety & Documentation

Safety Information

Hazard statements 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

BINOL and Derivatives

BINOL and its derivatives are one of the mostly widely used classes of ligands in asymmetric synthesis; being utilized in a broad array of reactions including: Diels–Alder, carbonyl addition and redu...
William Sommer and Daniel Weibel
Aldrich ChemFiles 2008, 8.2, 56.
Keywords: Addition reactions, Alkylations, Amidations, Asymmetric synthesis, Building blocks, Catalysis, Cycloadditions, Diels-Alder reaction, Ligands, Methods, Organic synthesis, Reductions

Chiral Diols

Apart from numerous examples using TADDOLs in metal-catalyzed asymmetric reactions, Rawal recently reported that TADDOLs could be used as Brønsted acid organocatalysts in highly stereoselective heter...
Aldrich ChemFiles 2007, 7.9, 13.
Keywords: Addition reactions, Aminations, Asymmetric synthesis, Catalysis, Chemfiles, Substitutions

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