Tetrakis[n-tetrachlorophthaloyl-(s)-tert-leucinato]dirhodium bis(ethyl acetate) adduct

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Reagent Code: #54255
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CAS Number 1816286-21-1

science Other reagents with same CAS 1816286-21-1

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Weight 1974.1700 g/mol
Formula C₅₆H₄₀Cl₁₆N₄O₁₆Rh₂
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Storage room temperature

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This chemical is primarily utilized as a highly efficient chiral catalyst in asymmetric synthesis, particularly in enantioselective reactions such as cyclopropanation, C-H functionalization, and carbene insertions. It is widely employed in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is crucial. Its application enables the synthesis of chiral intermediates with exceptional selectivity. Additionally, it is used in academic and industrial research to develop novel methodologies for asymmetric transformations, contributing to advancements in organic chemistry and drug development.

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inventory 50mg
10-20 days ฿7,956.00

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Tetrakis[n-tetrachlorophthaloyl-(s)-tert-leucinato]dirhodium bis(ethyl acetate) adduct
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This chemical is primarily utilized as a highly efficient chiral catalyst in asymmetric synthesis, particularly in enantioselective reactions such as cyclopropanation, C-H functionalization, and carbene insertions. It is widely employed in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is crucial. Its application enables the synthesis of chiral intermediates with exceptional selectivity. Additionally, it is used in academic and industrial research to develo

This chemical is primarily utilized as a highly efficient chiral catalyst in asymmetric synthesis, particularly in enantioselective reactions such as cyclopropanation, C-H functionalization, and carbene insertions. It is widely employed in the production of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is crucial. Its application enables the synthesis of chiral intermediates with exceptional selectivity. Additionally, it is used in academic and industrial research to develop novel methodologies for asymmetric transformations, contributing to advancements in organic chemistry and drug development.

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