(4S,4''S)-2,2''-(1-Phenylpropane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole) (S)-BnPh-SaBOX

95%

Reagent Code: #96557
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CAS Number 1404433-37-9

science Other reagents with same CAS 1404433-37-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 410.51 g/mol
Formula C₂₇H₂₆N₂O₂
badge Registry Numbers
MDL Number MFCD27978386
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis reactions. It is highly effective in coordinating with transition metals to form catalysts that facilitate the production of chiral molecules with high enantiomeric purity. Its application is prominent in the synthesis of pharmaceuticals, where the creation of single-enantiomer compounds is crucial for drug efficacy and safety. Additionally, it is employed in organic synthesis for constructing complex molecular architectures with precise stereochemical control, making it valuable in the development of fine chemicals and agrochemicals. Its robust structure and ability to induce high stereoselectivity make it a preferred choice in advanced synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,850.00
inventory 1g
10-20 days ฿22,095.00

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(4S,4''S)-2,2''-(1-Phenylpropane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole) (S)-BnPh-SaBOX
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis reactions. It is highly effective in coordinating with transition metals to form catalysts that facilitate the production of chiral molecules with high enantiomeric purity. Its application is prominent in the synthesis of pharmaceuticals, where the creation of single-enantiomer compounds is crucial for drug efficacy and safety. Additionally, it is employed in organic synthesis for co

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis reactions. It is highly effective in coordinating with transition metals to form catalysts that facilitate the production of chiral molecules with high enantiomeric purity. Its application is prominent in the synthesis of pharmaceuticals, where the creation of single-enantiomer compounds is crucial for drug efficacy and safety. Additionally, it is employed in organic synthesis for constructing complex molecular architectures with precise stereochemical control, making it valuable in the development of fine chemicals and agrochemicals. Its robust structure and ability to induce high stereoselectivity make it a preferred choice in advanced synthetic methodologies.

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