884879-23-6

Basic information

• Product Name: PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II)
• Synonyms: Chloro[(1,2,3-η)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl)iMidazol-2-ylidene]palladiuM(II),97%;Umicore CX31;UMicore CX31, 16% Pd, Product of UMicore;CX 31;ANTI-CONNEXIN 31(C-TERMINAL) antibody produced in rabbit;Gap junction beta-3 protein;GJB3;Chloro[(1,2,3-η)-3-phenyl-2-propenyl][1,3-bis(2,6-di-i-propylphenyl)imidazol-2-ylidene]palladium(II)
• CAS NO: 884879-23-6
• Molecular Formula: Neolyst CX31
• Molecular Weight: 0
• Product Categories: Pd;organometallic complex
• Mol File: 884879-23-6.mol
• Article Data: 0

Chemical Properties

• Melting Point: 205-208°C
• Appearance: /
• Storage Temp.: -20°C
• CAS DataBase Reference: PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II)(CAS DataBase Reference)
• NIST Chemistry Reference: PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II)(884879-23-6)
• EPA Substance Registry System: PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II)(884879-23-6)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/38
• Safety Statements: 22-24/25-26-36/37
• WGK Germany: 3
• Hazardous Substances Data: 884879-23-6(Hazardous Substances Data)

Usage

Description

PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II) is a yellow crystalline compound that serves as a versatile catalyst in various organic synthesis reactions. It is characterized by its unique structure, which includes a phenylallylchloro group and a 1,3-bis(diisopropylphenyl)imidazole-2-ylidene ligand, providing it with distinct catalytic properties.

Uses

Used in Pharmaceutical Industry:
PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II) is used as a catalyst for Suzuki-Miyaura couplings and Buchwald-Hartwig couplings, which are essential reactions in the synthesis of various pharmaceutical compounds. These coupling reactions allow for the formation of carbon-carbon and carbon-nitrogen bonds, respectively, enabling the creation of complex molecular structures with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II) is employed as a catalyst to facilitate Suzuki-Miyaura couplings and Buchwald-Hartwig couplings. These reactions are crucial for the formation of new chemical bonds and the synthesis of a wide range of organic compounds, including pharmaceuticals, agrochemicals, and advanced materials.
Used in Research and Development:
PHENYLALLYLCHLORO-[1,3-BIS(DIISOPROPYLPHENYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(II) is utilized in research and development settings as a catalyst for exploring new synthetic pathways and optimizing existing ones. Its unique properties make it a valuable tool for chemists working on the design and synthesis of novel compounds with potential applications in various industries.

Reactions

Catalyst used for room temperature Suzuki-Miyaura couplings. Catalyst used for rapid, room temperature Buchwald-Hartwig and Suzuki-Miyaura coupling reactions.