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DI-M-CHLOROBIS[2-[1-[(4-METHYLPHENYL)IMINO]ETHYL]FERROCENYL-C,N]DI-PALLADIUM is a complex chemical compound featuring two palladium atoms connected by a ferrocene-based ligand. The molecule also incorporates a chloro group and a 4-methylphenylimino group, which facilitate the formation of coordination bonds with other molecules. DI-M-CHLOROBIS[2-[1-[(4-METHYLPHENYL)IMINO]ETHYL]FERROCENYL-C,N]DI-PALLADIUM is renowned for its catalytic properties, making it an indispensable catalyst in a variety of organic synthesis reactions.

156279-08-2

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156279-08-2 Usage

Uses

Used in Organic Synthesis:
DI-M-CHLOROBIS[2-[1-[(4-METHYLPHENYL)IMINO]ETHYL]FERROCENYL-C,N]DI-PALLADIUM is used as a catalyst in organic synthesis for its ability to facilitate cross-coupling reactions and other molecular transformations. Its unique structure allows it to efficiently catalyze reactions, leading to the formation of new chemical compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, DI-M-CHLOROBIS[2-[1-[(4-METHYLPHENYL)IMINO]ETHYL]FERROCENYL-C,N]DI-PALLADIUM is utilized as a catalyst for the synthesis of complex organic molecules that are precursors to various pharmaceutical drugs. Its catalytic properties enable the production of these compounds with high efficiency and selectivity, contributing to the development of novel therapeutic agents.
Used in Material Science:
DI-M-CHLOROBIS[2-[1-[(4-METHYLPHENYL)IMINO]ETHYL]FERROCENYL-C,N]DI-PALLADIUM is also employed in material science as a catalyst for the synthesis of advanced materials with unique properties. Its ability to catalyze specific reactions allows for the creation of materials with tailored characteristics, such as improved conductivity, stability, or reactivity, which are essential for various applications in fields like electronics, energy, and environmental technology.
Used in Research and Development:
In research and development, DI-M-CHLOROBIS[2-[1-[(4-METHYLPHENYL)IMINO]ETHYL]FERROCENYL-C,N]DI-PALLADIUM serves as a valuable tool for exploring new chemical reactions and mechanisms. Its catalytic properties enable researchers to investigate novel synthetic pathways and develop innovative strategies for the synthesis of complex organic compounds, advancing the frontiers of chemical science.

Check Digit Verification of cas no

The CAS Registry Mumber 156279-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,2,7 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 156279-08:
(8*1)+(7*5)+(6*6)+(5*2)+(4*7)+(3*9)+(2*0)+(1*8)=152
152 % 10 = 2
So 156279-08-2 is a valid CAS Registry Number.

156279-08-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name DI-M-CHLOROBIS[2-[1-[(4-METHYLPHENYL)IMINO]ETHYL]FERROCENYL-C,N]DI-PALLADIUM

1.2 Other means of identification

Product number -
Other names [C5H5FeC5H3PdClC(CH3)NC6H4CH3-p]2

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:156279-08-2 SDS

156279-08-2Upstream product

156279-08-2Relevant academic research and scientific papers

Resolution of a cyclopalladated ferrocenylketimine

Wu, Yang Jie,Cui, Xiu Ling,Du, Chen Xia,Wang, Wen Ling,Guo, Rui Yun,Chen, Rong Feng

, p. 3727 - 3730 (2007/10/03)

The cyclopalladated ferrocenylketimine, [{Pd[(η5-C5C5)Fe{η5-C 5H3C(CH3)=N(C6H4CH 3-4)}](μ-Cl)}2] 1 was resolved into optically active diastereomers by using (S)-leucine as chiral auxiliary. The new optically active (S)-leucinato complexes of PdII containing ferrocenylketimine could be converted into optically active dimers with the same absolute configurations in the ferrocene moiety. The structure of the chiral dimer (Rp,Rp)-1 was determined by X-ray diffraction, on the basis of which the absolute configurations of all the optically active compounds studied were ascertained.

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