628339-96-8 Usage
Uses
Used in Pharmaceutical Industry:
Trans-Bis(dicyclohexylaMine)palladium(II) acetate, DAPCy, is used as a catalyst for the synthesis of complex organic molecules, which are often found in pharmaceutical compounds. Its ability to promote cross-coupling reactions allows for the creation of diverse and intricate molecular structures, contributing to the development of new drugs and therapies.
Used in Chemical Synthesis:
Trans-Bis(dicyclohexylaMine)palladium(II) acetate, DAPCy, is used as a catalyst for the coupling of aryl iodides with triarylbismuths, enabling the formation of new carbon-carbon bonds. This application is crucial in the synthesis of various organic compounds, including those with potential applications in materials science and pharmaceuticals.
Used in Material Science:
Trans-Bis(dicyclohexylaMine)palladium(II) acetate, DAPCy, is used as a catalyst in the synthesis of 3,6-diphenyl-9-hexyl-9H-carazole derivatives. These derivatives are important components in the development of advanced materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to their unique electronic and optical properties.
Used in Polymer Science:
Trans-Bis(dicyclohexylaMine)palladium(II) acetate, DAPCy, is used as a catalyst in the Suzuki coupling of dihexylfluorene derivatives. This reaction is essential for the synthesis of conjugated polymers, which are widely used in the development of advanced materials for applications such as flexible electronics, sensors, and energy storage devices.
Used in Organic Chemistry:
Trans-Bis(dicyclohexylaMine)palladium(II) acetate, DAPCy, is used as a catalyst in the Suzuki-Miyaura coupling of dibromopyrone with boronic acids. This reaction is a key step in the synthesis of various organic compounds, including those with potential applications in pharmaceuticals, agrochemicals, and other specialty chemicals.
Reaction
Pd-catalyzed coupling of aryl iodides with triarylbismuths.
Pd-catalyzed Suzuki Coupling Reactions of aryl bromides under mild aerobic conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 628339-96-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,8,3,3 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 628339-96:
(8*6)+(7*2)+(6*8)+(5*3)+(4*3)+(3*9)+(2*9)+(1*6)=188
188 % 10 = 8
So 628339-96-8 is a valid CAS Registry Number.
