(2-(1,3-Dioxolan-2-yl)phenyl)dicyclohexylphosphine

≥97%

Reagent Code: #68755
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CAS Number 246158-59-8

science Other reagents with same CAS 246158-59-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.45 g/mol
Formula C₂₁H₃₁O₂P
badge Registry Numbers
MDL Number MFCD07784367
thermostat Physical Properties
Melting Point 82-85 °C
Boiling Point 469.4±40.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, combining a dioxolane group with a phosphine moiety, enhances its ability to stabilize metal complexes, making it valuable in asymmetric synthesis. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it improves selectivity and yield. Additionally, its application extends to the development of pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. The ligand's robustness and versatility make it a preferred choice in organic synthesis and industrial catalysis.

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inventory 1g
10-20 days ฿9,612.00

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(2-(1,3-Dioxolan-2-yl)phenyl)dicyclohexylphosphine
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This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, combining a dioxolane group with a phosphine moiety, enhances its ability to stabilize metal complexes, making it valuable in asymmetric synthesis. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it improves selectivity and yield. Additionally, its application extends to the development of pharmaceuticals and fine c
This chemical is primarily used as a ligand in catalytic processes, particularly in transition metal-catalyzed reactions. Its unique structure, combining a dioxolane group with a phosphine moiety, enhances its ability to stabilize metal complexes, making it valuable in asymmetric synthesis. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it improves selectivity and yield. Additionally, its application extends to the development of pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. The ligand's robustness and versatility make it a preferred choice in organic synthesis and industrial catalysis.
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