(R)-()-5,5'-Bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxole

>95.0%(HPLC)

Reagent Code: #68804
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CAS Number 850253-53-1

science Other reagents with same CAS 850253-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 722.78700 g/mol
Formula C₄₆H₄₄O₄P₂
badge Registry Numbers
MDL Number MFCD09753008
thermostat Physical Properties
Melting Point 256-261 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry make it highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other key synthetic processes. It is especially valued in the pharmaceutical industry for the production of chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, its application extends to fine chemical synthesis, where it enhances the efficiency and selectivity of complex organic reactions.

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Test Parameter Specification
Purity 95-100%
Appearance White to beige; solid, powder, crystals, crystalline powder and/or chunks

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,100.00
inventory 200mg
10-20 days ฿2,990.00

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(R)-()-5,5'-Bis[di(3,5-xylyl)phosphino]-4,4'-bi-1,3-benzodioxole
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry make it highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other key synthetic processes. It is especially valued in the pharmaceutical industry for the production of chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. A

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry make it highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other key synthetic processes. It is especially valued in the pharmaceutical industry for the production of chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, its application extends to fine chemical synthesis, where it enhances the efficiency and selectivity of complex organic reactions.

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