(2S,3S)-2-Benzyl-3-(tert-butyl)-4-(2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%,>99% ee

Reagent Code: #68623
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CAS Number 1373432-13-3

science Other reagents with same CAS 1373432-13-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 420.48 g/mol
Formula C₂₆H₂₉O₃P
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

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 a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. Additionally, its sterically hindered tert-butyl group and benzyl substituents enhance its stability and selectivity in catalytic processes. This compound is also explored in material science for developing advanced chiral materials with potential applications in sensors or optoelectronic devices.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,182.00
inventory 500mg
10-20 days ฿28,782.00

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(2S,3S)-2-Benzyl-3-(tert-butyl)-4-(2,6-dimethoxyphenyl)-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 a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. Additionally, its sterically hinder

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 a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, which are crucial for producing optically active compounds. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is essential. Additionally, its sterically hindered tert-butyl group and benzyl substituents enhance its stability and selectivity in catalytic processes. This compound is also explored in material science for developing advanced chiral materials with potential applications in sensors or optoelectronic devices.

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