(2R,5R)-1-(2-(1,3-Dioxolan-2-yl)phenyl)-2,5-dimethylphospholane

97%, 99%ee

Reagent Code: #68618
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CAS Number 1044256-04-3

science Other reagents with same CAS 1044256-04-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.3 g/mol
Formula C₁₅H₂₁O₂P
badge Registry Numbers
MDL Number MFCD09842713
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a key ligand in transition metal-catalyzed reactions, such as hydrogenation, which is critical in the production of chiral pharmaceuticals. Its unique structure allows it to effectively control the stereochemistry of the reaction, leading to the formation of enantiomerically pure compounds. This makes it valuable in the synthesis of active pharmaceutical ingredients (APIs) where specific chirality is essential for biological activity. Additionally, it finds application in the development of advanced materials and fine chemicals, where precise molecular control is necessary.

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Size Availability Unit Price Quantity
inventory 1 g
10-20 days ฿20,475.00
inventory 250 mg
10-20 days ฿6,399.00
inventory 5 g
10-20 days ฿82,548.00

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(2R,5R)-1-(2-(1,3-Dioxolan-2-yl)phenyl)-2,5-dimethylphospholane
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This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a key ligand in transition metal-catalyzed reactions, such as hydrogenation, which is critical in the production of chiral pharmaceuticals. Its unique structure allows it to effectively control the stereochemistry of the reaction, leading to the formation of enantiomerically pure compounds. This makes it valuable in the synthesis of active pharmaceutical

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a key ligand in transition metal-catalyzed reactions, such as hydrogenation, which is critical in the production of chiral pharmaceuticals. Its unique structure allows it to effectively control the stereochemistry of the reaction, leading to the formation of enantiomerically pure compounds. This makes it valuable in the synthesis of active pharmaceutical ingredients (APIs) where specific chirality is essential for biological activity. Additionally, it finds application in the development of advanced materials and fine chemicals, where precise molecular control is necessary.

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