[1-(2R,5R)-2,5-dimethylphospholanyl]-[2-(2R,5R)-2,5-dimethylphospholanyl-1-oxide]benzene

98%, 99%ee

Reagent Code: #68617
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CAS Number 638132-66-8

science Other reagents with same CAS 638132-66-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.36 g/mol
Formula C₁₈H₂₈OP₂
badge Registry Numbers
MDL Number MFCD09750450
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring phospholane rings, makes it highly effective in inducing enantioselectivity, which is crucial for producing chiral molecules in pharmaceuticals and fine chemicals. It is often employed in hydrogenation reactions, where it helps generate optically active compounds with high precision. Additionally, its stability and ability to form robust complexes with metals like rhodium and iridium enhance its utility in industrial-scale synthesis of complex organic molecules. Its application extends to the production of active pharmaceutical ingredients (APIs) and other high-value chiral intermediates.

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Size Availability Unit Price Quantity
inventory 1 g
10-20 days ฿18,612.00
inventory 250 mg
10-20 days ฿5,823.00
inventory 5 g
10-20 days ฿75,042.00

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[1-(2R,5R)-2,5-dimethylphospholanyl]-[2-(2R,5R)-2,5-dimethylphospholanyl-1-oxide]benzene
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring phospholane rings, makes it highly effective in inducing enantioselectivity, which is crucial for producing chiral molecules in pharmaceuticals and fine chemicals. It is often employed in hydrogenation reactions, where it helps generate optically active compounds with high precision. Additionally, its stability and ability to form robust com

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring phospholane rings, makes it highly effective in inducing enantioselectivity, which is crucial for producing chiral molecules in pharmaceuticals and fine chemicals. It is often employed in hydrogenation reactions, where it helps generate optically active compounds with high precision. Additionally, its stability and ability to form robust complexes with metals like rhodium and iridium enhance its utility in industrial-scale synthesis of complex organic molecules. Its application extends to the production of active pharmaceutical ingredients (APIs) and other high-value chiral intermediates.

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