(S)-2,2'-Bis[bis(4-methoxy-3,5-di-t-butylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

98%

Reagent Code: #37996
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CAS Number 1365531-99-2

science Other reagents with same CAS 1365531-99-2

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Weight 1211.6100 g/mol
Formula C₇₆H₁₀₈O₈P₂
badge Registry Numbers
MDL Number MFCD20265636
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes. Its sterically hindered and electron-rich structure enhances selectivity and reactivity, making it valuable in the synthesis of pharmaceuticals, fine chemicals, and other chiral compounds. The ligand’s robustness and ability to induce high enantiomeric excesses are critical for producing optically pure substances in industrial and academic research settings.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,220.00

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(S)-2,2'-Bis[bis(4-methoxy-3,5-di-t-butylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes. Its sterically hindered and electron-rich structure enhances selectivity and reactivity, making it valuable in the synthesis of pharmaceuticals, fine chemicals, and other chiral compounds. The ligand’s robustness and

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes. Its sterically hindered and electron-rich structure enhances selectivity and reactivity, making it valuable in the synthesis of pharmaceuticals, fine chemicals, and other chiral compounds. The ligand’s robustness and ability to induce high enantiomeric excesses are critical for producing optically pure substances in industrial and academic research settings.

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