(S)-3,3′-Bis(9-anthracenyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate

98%, ee 99%

Reagent Code: #38361
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CAS Number 361342-52-1

science Other reagents with same CAS 361342-52-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 702 g/mol
Formula C₄₈H₃₀O₄P
thermostat Physical Properties
Melting Point >400°C
inventory_2 Storage & Handling
Density 1.46±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This chiral phosphoric acid derivative is primarily employed as a Brønsted acid catalyst in asymmetric organocatalysis, facilitating enantioselective reactions including aza-Mannich, Pictet-Spengler, and other carbon-carbon or carbon-heteroatom bond formations. Its distinctive (S)-binaphthyl backbone with 3,3'-anthracenyl substituents enhances stereoselectivity and catalytic efficiency. Furthermore, it serves in the synthesis of chiral stationary phases for high-performance liquid chromatography (HPLC), supporting enantiomer separation in pharmaceutical and fine chemical research. The fluorescent anthracene groups enable applications in molecular recognition and chemosensing studies.

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Test Parameter Specification
Appearance White to Yellow Powder or Crystals
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5 mg
10-20 days ฿1,845.00
inventory 100 mg
10-20 days ฿7,542.00
inventory 25 mg
10-20 days ฿4,266.00
inventory 250 mg
10-20 days ฿15,192.00

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(S)-3,3′-Bis(9-anthracenyl)-1,1′-binaphthyl-2,2′-diyl hydrogenphosphate
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This chiral phosphoric acid derivative is primarily employed as a Brønsted acid catalyst in asymmetric organocatalysis, facilitating enantioselective reactions including aza-Mannich, Pictet-Spengler, and other carbon-carbon or carbon-heteroatom bond formations. Its distinctive (S)-binaphthyl backbone with 3,3'-anthracenyl substituents enhances stereoselectivity and catalytic efficiency. Furthermore, it serves in the synthesis of chiral stationary phases for high-performance liquid chromatography (HPLC),

This chiral phosphoric acid derivative is primarily employed as a Brønsted acid catalyst in asymmetric organocatalysis, facilitating enantioselective reactions including aza-Mannich, Pictet-Spengler, and other carbon-carbon or carbon-heteroatom bond formations. Its distinctive (S)-binaphthyl backbone with 3,3'-anthracenyl substituents enhances stereoselectivity and catalytic efficiency. Furthermore, it serves in the synthesis of chiral stationary phases for high-performance liquid chromatography (HPLC), supporting enantiomer separation in pharmaceutical and fine chemical research. The fluorescent anthracene groups enable applications in molecular recognition and chemosensing studies.

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