(2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2-isopropyl-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%,≥99% ee

Reagent Code: #97047
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CAS Number 1891002-61-1

science Other reagents with same CAS 1891002-61-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 412.5 g/mol
Formula C₂₈H₂₉OP
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring an anthracene group and a phosphole ring, makes it effective in facilitating stereoselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where controlling stereochemistry is crucial. Additionally, its rigid framework and electron-rich properties make it suitable for applications in materials science, such as in the development of organic electronic devices or as a component in luminescent materials.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿39,591.00
inventory 100mg
10-20 days ฿8,991.00
inventory 25mg
10-20 days ฿3,591.00

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(2S,3S)-4-(Anthracen-9-yl)-3-(tert-butyl)-2-isopropyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring an anthracene group and a phosphole ring, makes it effective in facilitating stereoselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where controlling stereochemistry is crucial. Additionally, its rigid framewo

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring an anthracene group and a phosphole ring, makes it effective in facilitating stereoselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the synthesis of complex molecules, including pharmaceuticals, where controlling stereochemistry is crucial. Additionally, its rigid framework and electron-rich properties make it suitable for applications in materials science, such as in the development of organic electronic devices or as a component in luminescent materials.

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