RuPhos Pd G4

98%

Reagent Code: #126704
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Alias Methanesulfonic acid (2-dicyclohexylphosphino-2',4',6'-tri-isopropyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl- 2-yl) palladium(II)
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CAS Number 1599466-85-9

science Other reagents with same CAS 1599466-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 850.39 g/mol
Formula C₄₄H₅₈NO₅PPdS
thermostat Physical Properties
Melting Point 240°C
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

RuPhos Pd G4 is widely used in cross-coupling reactions, particularly in the pharmaceutical industry, due to its high efficiency and stability. It is effective in Suzuki-Miyaura and Buchwald-Hartwig amination reactions, enabling the synthesis of complex organic molecules and drug intermediates. Its robust performance at low catalyst loadings makes it a cost-effective choice for large-scale production. Additionally, it is utilized in the development of agrochemicals and fine chemicals, where precise and reliable coupling reactions are essential. The catalyst’s compatibility with a wide range of functional groups further enhances its versatility in organic synthesis.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms To Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿7,290.00
250mg
10-20 days ฿1,980.00
RuPhos Pd G4
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RuPhos Pd G4 is widely used in cross-coupling reactions, particularly in the pharmaceutical industry, due to its high efficiency and stability. It is effective in Suzuki-Miyaura and Buchwald-Hartwig amination reactions, enabling the synthesis of complex organic molecules and drug intermediates. Its robust performance at low catalyst loadings makes it a cost-effective choice for large-scale production. Additionally, it is utilized in the development of agrochemicals and fine chemicals, where precise and r

RuPhos Pd G4 is widely used in cross-coupling reactions, particularly in the pharmaceutical industry, due to its high efficiency and stability. It is effective in Suzuki-Miyaura and Buchwald-Hartwig amination reactions, enabling the synthesis of complex organic molecules and drug intermediates. Its robust performance at low catalyst loadings makes it a cost-effective choice for large-scale production. Additionally, it is utilized in the development of agrochemicals and fine chemicals, where precise and reliable coupling reactions are essential. The catalyst’s compatibility with a wide range of functional groups further enhances its versatility in organic synthesis.

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