(Sa,S)-DTB-Ph-SIPHOX

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Reagent Code: #68666
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CAS Number 1040274-12-1

science Other reagents with same CAS 1040274-12-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 774.06 g/mol
Formula C₅₄H₆₄NOP
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with specific stereochemistry. The ligand’s structure allows it to effectively coordinate with metals like rhodium or iridium, enhancing the enantioselectivity of reactions such as hydrogenation, allylic alkylation, and hydroformylation. This makes it a valuable tool in the development of active pharmaceutical ingredients (APIs) and fine chemicals, where precise stereochemical control is essential for efficacy and safety. Additionally, it is employed in academic and industrial research to explore new catalytic processes and optimize existing ones for higher selectivity and yield.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,550.00

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(Sa,S)-DTB-Ph-SIPHOX
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with specific stereochemistry. The ligand’s structure allows it to effectively coordinate with metals like rhodium or iridium, enhancing the enantioselectivity of reactions such as hydrogenation, allylic alkylation, and hy

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its application is significant in the synthesis of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for producing drugs with specific stereochemistry. The ligand’s structure allows it to effectively coordinate with metals like rhodium or iridium, enhancing the enantioselectivity of reactions such as hydrogenation, allylic alkylation, and hydroformylation. This makes it a valuable tool in the development of active pharmaceutical ingredients (APIs) and fine chemicals, where precise stereochemical control is essential for efficacy and safety. Additionally, it is employed in academic and industrial research to explore new catalytic processes and optimize existing ones for higher selectivity and yield.

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