BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)PHOSPHINE

Reagent Code: #122267
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CAS Number 166172-69-6

science Other reagents with same CAS 166172-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 458.18 g/mol
Formula C₁₆H₇F₁₂P
badge Registry Numbers
MDL Number MFCD01630858
thermostat Physical Properties
Melting Point 69-73 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. Its electron-withdrawing trifluoromethyl groups enhance the stability and reactivity of the metal complexes, making it valuable in cross-coupling reactions, hydrogenation, and other organometallic transformations. It is also employed in the synthesis of fine chemicals and pharmaceuticals, where precise control over reaction pathways is crucial. Additionally, its unique steric and electronic properties make it suitable for use in asymmetric catalysis, aiding in the production of enantiomerically pure compounds.

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Test Parameter Specification
Appearance White to beige solid, powder, crystals, crystalline powder and/or chunks
Infrared Spectrum Conforms to Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,160.00

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BIS(3,5-DI(TRIFLUOROMETHYL)PHENYL)PHOSPHINE
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This chemical is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. Its electron-withdrawing trifluoromethyl groups enhance the stability and reactivity of the metal complexes, making it valuable in cross-coupling reactions, hydrogenation, and other organometallic transformations. It is also employed in the synthesis of fine chemicals and pharmaceuticals, where precise control over reaction pathways is crucial. Additionally, its unique ste

This chemical is primarily utilized as a ligand in various catalytic processes, particularly in transition metal-catalyzed reactions. Its electron-withdrawing trifluoromethyl groups enhance the stability and reactivity of the metal complexes, making it valuable in cross-coupling reactions, hydrogenation, and other organometallic transformations. It is also employed in the synthesis of fine chemicals and pharmaceuticals, where precise control over reaction pathways is crucial. Additionally, its unique steric and electronic properties make it suitable for use in asymmetric catalysis, aiding in the production of enantiomerically pure compounds.

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