2-((2R,3R)-3-(tert-Butyl)-4-(3,5-dicyclopentyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphol-2-yl)propan-2-ol

97%,99% ee

Reagent Code: #41124
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CAS Number 2416226-97-4

science Other reagents with same CAS 2416226-97-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 524.69 g/mol
Formula C₃₂H₄₅O₄P
inventory_2 Storage & Handling
Storage room temperature, 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 dihydrobenzooxaphosphole core, makes it effective in promoting enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the pharmaceutical industry to synthesize enantiomerically pure compounds, which are crucial for developing drugs with high specificity and reduced side effects. Additionally, its tert-butyl and dicyclopentyl groups enhance steric hindrance, improving selectivity in catalytic processes. This chemical is also explored in material science for designing advanced chiral materials with potential applications in optoelectronics or sensors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿30,726.00
inventory 500mg
10-20 days ฿102,600.00
inventory 25mg
10-20 days ฿13,653.00

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2-((2R,3R)-3-(tert-Butyl)-4-(3,5-dicyclopentyl-2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphol-2-yl)propan-2-ol
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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 dihydrobenzooxaphosphole core, makes it effective in promoting enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the pharmaceutical industry to synthesize enantiomerically pure compounds, which are crucial for developing drugs with high specificity and reduced sid

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 dihydrobenzooxaphosphole core, makes it effective in promoting enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the pharmaceutical industry to synthesize enantiomerically pure compounds, which are crucial for developing drugs with high specificity and reduced side effects. Additionally, its tert-butyl and dicyclopentyl groups enhance steric hindrance, improving selectivity in catalytic processes. This chemical is also explored in material science for designing advanced chiral materials with potential applications in optoelectronics or sensors.

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