Determine the necessary mass, volume, or concentration for preparing a solution.
≥99.95% metals basis for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product class
M-P, Homogeneous Catalysts, M-O, Acetate Ligands, Phosphorus Ligands - Chiral
Reaction type
Hydrogenation, Asymmetric Reactions, Asymmetric Hydrogenation, Transfer Hydrogenation
Chemical properties
C42H38O6P2Ru
Ru[(R)-MeO-BIPHEP](OAc)2
801.78
Ru
13
powder
yellow
99.95
Applications & references
Asymmetric hydrogenation of (Z)-methyl 3-amino-4-methoxy butenoate.
Reference: Org. Proc. Res. Dev. 2011, 15, 353 (DOI: 10.1021/op034181b)
Synthesis of (S)-fluoromethyldihydro-furan-2-one for the manufacture of pyrido[2,1-a]isoquinoline derivatives which are useful for treatment or prophylaxis of diseases.
Reference: WO2006 125728
Asymmetric hydrogenation of (3R,4R)-4-hydroxy-azepane-3-carboxylic acid ethyl ester for the synthesis of well-known pharmacologically active compounds, e.g. balanol.
Reference: EP0802190
Asymmetric hydrogenation and enantioselective hydrogen-shift in prochiral allylic systems.
Reference: EP0398132
| Peso molecolare | 801.78 |
|---|
Comprehensive hazard, handling, storage, and regulatory compliance document.
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