R-3,3'-Dibromo-1,1'-binaphthyl-2,2'-diylhydrogenphosphate

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Reagent Code: #231169
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CAS Number 861909-33-3

science Other reagents with same CAS 861909-33-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 506.08 g/mol
Formula C₂₀H₁₁Br₂O₄P
badge Registry Numbers
MDL Number MFCD25372845
thermostat Physical Properties
Boiling Point 693.9±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.95±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral catalyst or chiral auxiliary in asymmetric synthesis, particularly in enantioselective phosphorylation and esterification reactions. Its binaphthyl backbone provides a rigid, sterically hindered environment that enhances stereoselectivity. Commonly employed in the preparation of chiral phosphates and phosphonates, which are key intermediates in pharmaceuticals and biologically active compounds. Also utilized in coordination chemistry as a ligand for transition metals in asymmetric catalysis. Shows utility in the development of chiral sensors and materials for enantiomeric recognition.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,040.00
250mg
10-20 days ฿6,090.00
1g
10-20 days ฿19,070.00
5g
10-20 days ฿89,500.00

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R-3,3'-Dibromo-1,1'-binaphthyl-2,2'-diylhydrogenphosphate
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Used as a chiral catalyst or chiral auxiliary in asymmetric synthesis, particularly in enantioselective phosphorylation and esterification reactions. Its binaphthyl backbone provides a rigid, sterically hindered environment that enhances stereoselectivity. Commonly employed in the preparation of chiral phosphates and phosphonates, which are key intermediates in pharmaceuticals and biologically active compounds. Also utilized in coordination chemistry as a ligand for transition metals in asymmetric cataly

Used as a chiral catalyst or chiral auxiliary in asymmetric synthesis, particularly in enantioselective phosphorylation and esterification reactions. Its binaphthyl backbone provides a rigid, sterically hindered environment that enhances stereoselectivity. Commonly employed in the preparation of chiral phosphates and phosphonates, which are key intermediates in pharmaceuticals and biologically active compounds. Also utilized in coordination chemistry as a ligand for transition metals in asymmetric catalysis. Shows utility in the development of chiral sensors and materials for enantiomeric recognition.

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