1,1'-Bis[(11bR)-3,5-dihydro-4H-dinaphtho[2,1-c:1',2'-e]phosphepin-4-yl]ferrocene

97%

Reagent Code: #38723
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CAS Number 328395-00-2

science Other reagents with same CAS 328395-00-2

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Weight 798.6244 g/mol
Formula C₅₄H₃₂FeP₂
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Storage room temperature

description Product Description

This chemical is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a ferrocene backbone and chiral phosphine ligands, makes it highly effective in enantioselective transformations. It is often employed in hydrogenation reactions, where it facilitates the production of optically active compounds with high selectivity. Additionally, it finds applications in cross-coupling reactions, enabling the formation of carbon-carbon bonds in a stereocontrolled manner. Its robustness and efficiency make it a valuable tool in pharmaceutical and fine chemical industries for the synthesis of complex chiral intermediates.

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inventory 50mg
10-20 days ฿3,762.00

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1,1'-Bis[(11bR)-3,5-dihydro-4H-dinaphtho[2,1-c:1',2'-e]phosphepin-4-yl]ferrocene
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This chemical is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a ferrocene backbone and chiral phosphine ligands, makes it highly effective in enantioselective transformations. It is often employed in hydrogenation reactions, where it facilitates the production of optically active compounds with high selectivity. Additionally, it finds applications in cross-coupling reactions, enabling the formation of carbon-ca

This chemical is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a ferrocene backbone and chiral phosphine ligands, makes it highly effective in enantioselective transformations. It is often employed in hydrogenation reactions, where it facilitates the production of optically active compounds with high selectivity. Additionally, it finds applications in cross-coupling reactions, enabling the formation of carbon-carbon bonds in a stereocontrolled manner. Its robustness and efficiency make it a valuable tool in pharmaceutical and fine chemical industries for the synthesis of complex chiral intermediates.

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