(R)-(-)-2,2'-Bis[di(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl

98%

Reagent Code: #37263
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CAS Number 352655-40-4

science Other reagents with same CAS 352655-40-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1091.5161 g/mol
Formula C₇₀H₁₀₀N₄O₂P₂
badge Registry Numbers
MDL Number MFCD09753010
inventory_2 Storage & Handling
Storage 2-8°C

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 high stereochemical precision. The ligand’s unique structure, featuring bulky substituents and methoxy groups, enhances its ability to induce high enantioselectivity in reactions such as hydrogenation, cross-coupling, and allylic substitution. Its effectiveness in these processes makes it valuable for creating complex molecules with specific chiral configurations, essential for developing active pharmaceutical ingredients (APIs) and fine chemicals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,750.00
inventory 250mg
10-20 days ฿8,450.00
inventory 1g
10-20 days ฿33,770.00

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(R)-(-)-2,2'-Bis[di(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl
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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 high stereochemical precision. The ligand’s unique structure, featuring bulky substituents and methoxy groups, enhances its ability to induce high enantioselectivity in reactions such as hydrogenation, cross-coupling,

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 high stereochemical precision. The ligand’s unique structure, featuring bulky substituents and methoxy groups, enhances its ability to induce high enantioselectivity in reactions such as hydrogenation, cross-coupling, and allylic substitution. Its effectiveness in these processes makes it valuable for creating complex molecules with specific chiral configurations, essential for developing active pharmaceutical ingredients (APIs) and fine chemicals.

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