950982-69-1 Usage
Description
1-(2-bis(3,5-xylyl)phosphinoferrocenyl)ethylbis(3,5-xylyl)phosphine is a phosphine derivative featuring a ferrocenyl group attached to it. 1-(2-bis(3,5-xylyl)phosphinoferrocenyl)ethylbis(3,5-xylyl)phosphine is characterized by two phosphine groups connected by an ethyl bridge, with each phosphine atom having two 3,5-xylyl groups attached. The unique structure of this compound, particularly the presence of the ferrocenyl group, makes it a valuable ligand in organometallic chemistry, where it can aid in the coordination of metal ions. Additionally, its properties suggest potential applications in catalysis and material science, making it a versatile compound for various fields of chemistry and materials research.
Uses
Used in Organometallic Chemistry:
1-(2-bis(3,5-xylyl)phosphinoferrocenyl)ethylbis(3,5-xylyl)phosphine is used as a ligand for facilitating the coordination of metal ions in organometallic chemistry. Its unique structure, including the ferrocenyl group, enhances its ability to form stable complexes with metals, which can be beneficial in various chemical reactions and processes.
Used in Catalysis:
In the field of catalysis, 1-(2-bis(3,5-xylyl)phosphinoferrocenyl)ethylbis(3,5-xylyl)phosphine is used as a catalyst or a catalyst precursor. Its ability to coordinate with metal ions can enhance the efficiency of catalytic reactions, making it a valuable component in various industrial processes.
Used in Material Science:
1-(2-bis(3,5-xylyl)phosphinoferrocenyl)ethylbis(3,5-xylyl)phosphine is used in material science for the development of new materials with unique properties. Its structural characteristics and ability to coordinate with metal ions can contribute to the creation of advanced materials with potential applications in various industries, such as electronics, energy storage, and pharmaceuticals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(2-bis(3,5-xylyl)phosphinoferrocenyl)ethylbis(3,5-xylyl)phosphine may be used as a starting material or a component in the synthesis of new drugs. Its ability to form stable complexes with metal ions can be exploited in the development of novel therapeutic agents, particularly those targeting metal ion-related diseases or conditions.
Used in Environmental Applications:
1-(2-bis(3,5-xylyl)phosphinoferrocenyl)ethylbis(3,5-xylyl)phosphine can be employed in environmental applications, such as the remediation of metal-contaminated sites. Its ability to coordinate with metal ions can help in the sequestration and removal of toxic metals from the environment, contributing to cleaner and safer ecosystems.
Check Digit Verification of cas no
The CAS Registry Mumber 950982-69-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,9,8 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 950982-69:
(8*9)+(7*5)+(6*0)+(5*9)+(4*8)+(3*2)+(2*6)+(1*9)=211
211 % 10 = 1
So 950982-69-1 is a valid CAS Registry Number.
950982-69-1Relevant articles and documents
Tunable ferrocenyl diphosphine ligands for the Ir-catalyzed enantioselective hydrogenation of N-aryl imines
Blaser, Hans-Ulrich,Buser, Hans-Peter,H?usel, Robert,Jalett, Hans-Peter,Spindler, Felix
, p. 34 - 38 (2001)
Ferrocenyl diphosphines R2PF-P(R′)2 are effective, tunable ligands for the iridium catalyzed enantioselective hydrogenation of N-aryl imines in the presence of iodide and acid promoters. Structure-activity/selectivity correlations were found for the hydrogenation of N-(2-ethyl-6-methylphenyl)-N-(1′-methoxymethyl)-ethylidene-amine (MEA-imine) and for 2,3,3-trimethylindolenine (TMI). Extremely high catalytic activity and moderate to good enantioselectivity were observed for the MEA imine using a catalyst generated in situ from [Ir(cod)Cl]2 and (R)-(S)-PPF-P(3,5-Xyl)2 (xyliphos). With the same type of catalysts, several other N-aryl imines can be hydrogenated with enantioselectivities between 31 and 96%, albeit with lower catalyst activities.
