2'-Dicyclohexylphosphino-2,6-di-i-propyl-4-sulfonato-1,1'-biphenyl hydrate sodium salt

98%

Reagent Code: #76767
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CAS Number 870245-84-4

science Other reagents with same CAS 870245-84-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 536.68(anhydrous) g/mol
Formula C₃₀H₄₂NaO₃PSXH₂O
badge Registry Numbers
MDL Number MFCD09265103
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description Product Description

This chemical is widely used as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its sulfonated group enhances water solubility, making it suitable for aqueous-phase catalysis, which is advantageous for environmentally friendly and sustainable chemical processes. It is also employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to stabilize metal complexes and improve reaction efficiency. Additionally, its robust structure and electron-rich nature make it effective in asymmetric catalysis, enabling the production of chiral compounds with high enantioselectivity.

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Test Parameter Specification
Appearance Off-White to Light Yellow to Yellow Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿18,720.00
inventory 100mg
10-20 days ฿6,480.00

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2'-Dicyclohexylphosphino-2,6-di-i-propyl-4-sulfonato-1,1'-biphenyl hydrate sodium salt
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This chemical is widely used as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its sulfonated group enhances water solubility, making it suitable for aqueous-phase catalysis, which is advantageous for environmentally friendly and sustainable chemical processes. It is also employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to stabilize metal complexes and impro

This chemical is widely used as a ligand in transition metal-catalyzed reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Buchwald-Hartwig reactions. Its sulfonated group enhances water solubility, making it suitable for aqueous-phase catalysis, which is advantageous for environmentally friendly and sustainable chemical processes. It is also employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to stabilize metal complexes and improve reaction efficiency. Additionally, its robust structure and electron-rich nature make it effective in asymmetric catalysis, enabling the production of chiral compounds with high enantioselectivity.

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