(8α,9R)-(8''α,9''R)-9,9''-[(2,5-Diphenyl-4,6-pyrimidinediyl)bis(oxy)]bis[6'-methoxycinchonan]

≥98%,99%d.e.

Reagent Code: #70228
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CAS Number 189745-70-8

science Other reagents with same CAS 189745-70-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 877.1 g/mol
Formula C₅₆H₅₆N₆O₄
inventory_2 Storage & Handling
Density 1.30±0.1 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure allows it to facilitate enantioselective transformations, making it valuable in the production of pharmaceuticals and fine chemicals where specific stereochemistry is crucial. It is often employed in catalytic processes such as asymmetric hydrogenation, oxidation, or carbon-carbon bond formation, enabling the synthesis of complex molecules with high enantiomeric purity. Additionally, its application extends to the development of novel materials and intermediates in chemical research, where precise control over molecular chirality is required.

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inventory 1g
10-20 days ฿23,340.00

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(8α,9R)-(8''α,9''R)-9,9''-[(2,5-Diphenyl-4,6-pyrimidinediyl)bis(oxy)]bis[6'-methoxycinchonan]
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This compound is primarily utilized in the field of asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure allows it to facilitate enantioselective transformations, making it valuable in the production of pharmaceuticals and fine chemicals where specific stereochemistry is crucial. It is often employed in catalytic processes such as asymmetric hydrogenation, oxidation, or carbon-carbon bond formation, enabling the synthesis of complex molecules with h

This compound is primarily utilized in the field of asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. Its unique structure allows it to facilitate enantioselective transformations, making it valuable in the production of pharmaceuticals and fine chemicals where specific stereochemistry is crucial. It is often employed in catalytic processes such as asymmetric hydrogenation, oxidation, or carbon-carbon bond formation, enabling the synthesis of complex molecules with high enantiomeric purity. Additionally, its application extends to the development of novel materials and intermediates in chemical research, where precise control over molecular chirality is required.

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