(R)-2-diphenyphosphino,2'-hydroxyl-1,1'-binaphthyl

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Reagent Code: #57510
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CAS Number 149917-88-4

science Other reagents with same CAS 149917-88-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 454.4982 g/mol
Formula C₃₂H₂₃OP
badge Registry Numbers
MDL Number MFCD01166485
thermostat Physical Properties
Boiling Point 602.3±43.0 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of chiral molecules with high optical purity. Applications include hydrogenation, carbon-carbon bond formation, and other transformations in pharmaceutical and fine chemical industries. Its ability to induce chirality in products makes it valuable for synthesizing active pharmaceutical ingredients (APIs) and intermediates with specific stereochemistry. Additionally, it is employed in research and development to explore new catalytic processes and optimize reaction conditions for improved selectivity and efficiency.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,450.00

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(R)-2-diphenyphosphino,2'-hydroxyl-1,1'-binaphthyl
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of chiral molecules with high optical purity. Applications include hydrogenation, carbon-carbon bond formation, and other transformations in pharmaceutical and fine chemical industries. Its ability to induce chirality in products makes it valuable for synthesizing active pharmaceutical ingredients (API

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of chiral molecules with high optical purity. Applications include hydrogenation, carbon-carbon bond formation, and other transformations in pharmaceutical and fine chemical industries. Its ability to induce chirality in products makes it valuable for synthesizing active pharmaceutical ingredients (APIs) and intermediates with specific stereochemistry. Additionally, it is employed in research and development to explore new catalytic processes and optimize reaction conditions for improved selectivity and efficiency.

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