(S)-(7'-(Bis(3,5-di-tert-butylphenyl)phosphanyl)-2,2',3,3'-tetrahydro-1,1'-spirobi[inden]-7-yl)methanamine

98%

Reagent Code: #65662
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CAS Number 1403328-55-1

science Other reagents with same CAS 1403328-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 657.95 g/mol
Formula C₄₆H₆₀NP
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 the synthesis of enantiomerically pure compounds. Its unique structure, featuring a spirobi[inden] core and bulky phosphanyl groups, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed reactions. It is especially valuable in the pharmaceutical industry for producing chiral intermediates and active pharmaceutical ingredients (APIs) with high stereochemical purity. Additionally, its sterically demanding design enhances selectivity and efficiency in catalytic processes, making it a preferred choice for complex organic syntheses.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿7,920.00
inventory 50mg
10-20 days ฿32,040.00

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(S)-(7'-(Bis(3,5-di-tert-butylphenyl)phosphanyl)-2,2',3,3'-tetrahydro-1,1'-spirobi[inden]-7-yl)methanamine
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring a spirobi[inden] core and bulky phosphanyl groups, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed reactions. It is especially valuable in the pharmaceutical industry for producing chiral intermediates and active

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring a spirobi[inden] core and bulky phosphanyl groups, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed reactions. It is especially valuable in the pharmaceutical industry for producing chiral intermediates and active pharmaceutical ingredients (APIs) with high stereochemical purity. Additionally, its sterically demanding design enhances selectivity and efficiency in catalytic processes, making it a preferred choice for complex organic syntheses.

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