(11bR)​-8,​9,​10,​11,​12,​13,​14,​15-Octahydro-​4-​hydroxy-​2,​6-​di-​1-​pyrenyl-4-​oxide-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin

≥98%,99%e.e.

Reagent Code: #70299
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CAS Number 1225195-02-7

science Other reagents with same CAS 1225195-02-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 756.8 g/mol
Formula C₅₂H₃₇O₄P
inventory_2 Storage & Handling
Density 1.46±0.1 g/mL
Storage room temperature, dry

description Product Description

This chiral phosphine oxide is a specialty reagent primarily used as a ligand in asymmetric catalysis for organic synthesis. Featuring a binaphthyl-derived [1,3,2]dioxaphosphepin core with bulky 1-pyrenyl substituents and high enantiomeric purity (>99% e.e.), it enables highly stereoselective reactions, such as enantioselective C-C bond formations or reductions. Its stability and steric properties make it valuable in the preparation of enantiomerically pure intermediates for pharmaceuticals, agrochemicals, and advanced materials, including those for optoelectronics where chirality influences performance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿35,480.00

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(11bR)​-8,​9,​10,​11,​12,​13,​14,​15-Octahydro-​4-​hydroxy-​2,​6-​di-​1-​pyrenyl-4-​oxide-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin
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This chiral phosphine oxide is a specialty reagent primarily used as a ligand in asymmetric catalysis for organic synthesis. Featuring a binaphthyl-derived [1,3,2]dioxaphosphepin core with bulky 1-pyrenyl substituents and high enantiomeric purity (>99% e.e.), it enables highly stereoselective reactions, such as enantioselective C-C bond formations or reductions. Its stability and steric properties make it valuable in the preparation of enantiomerically pure intermediates for pharmaceuticals, agrochemi

This chiral phosphine oxide is a specialty reagent primarily used as a ligand in asymmetric catalysis for organic synthesis. Featuring a binaphthyl-derived [1,3,2]dioxaphosphepin core with bulky 1-pyrenyl substituents and high enantiomeric purity (>99% e.e.), it enables highly stereoselective reactions, such as enantioselective C-C bond formations or reductions. Its stability and steric properties make it valuable in the preparation of enantiomerically pure intermediates for pharmaceuticals, agrochemicals, and advanced materials, including those for optoelectronics where chirality influences performance.

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