(S)-3,3'-Bis(10-phenyl-9-anthracenyl)-1,1'-binaphthyl-2,2'-diyl Hydrogenphosphate

98%

Reagent Code: #233303
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CAS Number 2207600-84-6

science Other reagents with same CAS 2207600-84-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 852.93 g/mol
Formula C₆₀H₃₇O₄P
inventory_2 Storage & Handling
Density 1.43±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a chiral catalyst or chiral ligand in asymmetric synthesis, enabling high enantioselectivity in organic transformations such as phosphorylation reactions and carbon–carbon bond-forming reactions. Its binaphthyl backbone with bulky anthracenyl groups provides a rigid, sterically hindered environment that enhances stereochemical control. Commonly applied in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Also employed in advanced materials research due to its extended π-conjugated system, contributing to chiral optical properties useful in OLEDs and molecular recognition systems.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿16,710.00
inventory 100mg
10-20 days ฿22,520.00
inventory 250mg
10-20 days ฿37,490.00

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(S)-3,3'-Bis(10-phenyl-9-anthracenyl)-1,1'-binaphthyl-2,2'-diyl Hydrogenphosphate
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Used as a chiral catalyst or chiral ligand in asymmetric synthesis, enabling high enantioselectivity in organic transformations such as phosphorylation reactions and carbon–carbon bond-forming reactions. Its binaphthyl backbone with bulky anthracenyl groups provides a rigid, sterically hindered environment that enhances stereochemical control. Commonly applied in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Also employed in advanced materials research due to its extended π-c

Used as a chiral catalyst or chiral ligand in asymmetric synthesis, enabling high enantioselectivity in organic transformations such as phosphorylation reactions and carbon–carbon bond-forming reactions. Its binaphthyl backbone with bulky anthracenyl groups provides a rigid, sterically hindered environment that enhances stereochemical control. Commonly applied in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Also employed in advanced materials research due to its extended π-conjugated system, contributing to chiral optical properties useful in OLEDs and molecular recognition systems.

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