(R)-2-(2-(Bis(4-(trifluoromethyl)phenyl)phosphino)-5-(trifluoromethyl)phenyl)-4-(tert-butyl)-4,5-dihydrooxazole

98%

Reagent Code: #59690
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CAS Number 1006708-91-3

science Other reagents with same CAS 1006708-91-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 591.45 g/mol
Formula C₂₈H₂₃F₉NOP
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral molecules. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds. Its application is significant in the pharmaceutical industry, where it aids in the development of chiral drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in the fine chemicals sector for the synthesis of complex organic molecules with high stereoselectivity. The compound's unique structure, featuring trifluoromethyl groups, enhances its stability and reactivity in various catalytic processes, making it a valuable tool in advanced organic synthesis.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿7,290.00
inventory 50mg
10-20 days ฿27,774.00

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(R)-2-(2-(Bis(4-(trifluoromethyl)phenyl)phosphino)-5-(trifluoromethyl)phenyl)-4-(tert-butyl)-4,5-dihydrooxazole
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This compound is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral molecules. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds. Its application is significant in the pharmaceutical industry, where it aids in the development of chiral drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in the fine chemicals sector for the synthesis of complex organic molecules w

This compound is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral molecules. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds. Its application is significant in the pharmaceutical industry, where it aids in the development of chiral drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in the fine chemicals sector for the synthesis of complex organic molecules with high stereoselectivity. The compound's unique structure, featuring trifluoromethyl groups, enhances its stability and reactivity in various catalytic processes, making it a valuable tool in advanced organic synthesis.

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