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  • 683981 - (5aS,10bR)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H, 6H-indeno[2,1-b]-1,2,4-triazolo[4,3-d]-1,4-oxazinium chloride monohydrate

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683981 Aldrich

(5aS,10bR)-5a,10b-Dihydro-2-(2,4,6-trimethylphenyl)-4H, 6H-indeno[2,1-b]-1,2,4-triazolo[4,3-d]-1,4-oxazinium chloride monohydrate

97%

Synonym: Bode Catalyst 1

  • Empirical Formula (Hill Notation) C21H22ClN3O · H2O

  • Molecular Weight 385.89

  •  PubChem Substance ID 329760887

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Properties

Related Categories Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Other Organocatalysts
InChI Key   GUECWMLEUCWYOS-OZYANKIXSA-M
assay   97%
optical activity   [α]20/D -156.0°, c = 1 in chloroform
mp   212-216 °C

Description

Packaging

100, 250 mg in glass insert

Legal Information

Sold in collaboration with BioBlocks, Inc.

Price and Availability

Safety & Documentation

Safety Information

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

Articles

Jeffrey Bode Group – Professor Product Portal

From our library of Articles, Sigma-Aldrich presents Jeffrey Bode Group – Professor Product Portal
Keywords: Annulations, Asymmetric synthesis, Catalysis, Cross couplings, transformation

Shi Epoxidation Catalyst

This organocatalyst is able to epoxidize trans alkenes and certain cis alkenes with good to excellent yields and selectivities.
Aldrich ChemFiles 2007, 7.9, 22.
Keywords: Chemfiles

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