2179-89-7 Usage
Uses
Used in Organic Synthesis:
BIS(1,3-DIPHENYL-2-IMIDAZOLIDINYLIDENE) is used as a catalyst for facilitating various chemical reactions in organic synthesis. Its ability to form stable complexes with transition metals enhances the efficiency and selectivity of these reactions.
Used in Organometallic Chemistry:
In the field of organometallic chemistry, BIS(1,3-DIPHENYL-2-IMIDAZOLIDINYLIDENE) is utilized as a ligand in catalytic processes. Its role in these processes is crucial for the advancement of organometallic chemistry, where it contributes to the development of new catalysts and reactions.
Used in Medicinal Chemistry:
BIS(1,3-DIPHENYL-2-IMIDAZOLIDINYLIDENE) has been studied for its potential applications in medicinal chemistry. Its unique properties and reactivity make it a candidate for the development of new pharmaceutical compounds and drug delivery systems.
Used as a Polymer Stabilizer:
BIS(1,3-DIPHENYL-2-IMIDAZOLIDINYLIDENE) is also used as a stabilizer for polymers, enhancing their durability and performance in various applications. Its stabilizing properties are valuable in the plastics and materials industry, contributing to the creation of more robust and long-lasting products.
Check Digit Verification of cas no
The CAS Registry Mumber 2179-89-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2179-89:
(6*2)+(5*1)+(4*7)+(3*9)+(2*8)+(1*9)=97
97 % 10 = 7
So 2179-89-7 is a valid CAS Registry Number.
2179-89-7Relevant academic research and scientific papers
Synthesis of electron-rich platinum centers: Platinum0(carbene) (alkene)2 complexes
Duin, Marcel A.,Lutz, Martin,Spek, Anthony L.,Elsevier, Cornelis J.
, p. 5804 - 5815 (2007/10/03)
The synthesis and molecular structure of the zero-valent platinum-mono-carbene-bis-alkene complexes [Pt0(NHC)(dimethyl fumarate)2] (NHC = 1,3-dimesityl-imidazol-2-ylidene (1a); 1,3-dimesityl-dihydroimidazol-2-ylidene (2a); diphenyl-d
A general and versatile approach to thermally generated N-heterocyclic carbenes
Nyce, Gregory W.,Csihony, Szilard,Waymouth, Robert M.,Hedrick, James L.
, p. 4073 - 4079 (2007/10/03)
The synthesis of N-heterocyclic carbene (NHC) adducts by condensation of diamines with appropriately substituted benzaldehydes is described. This simplified approach provides the NHC adduct without first having to generate the carbene followed by its protection. These adducts undergo thermal deprotection to generate N-heterocyclic carbene in situ. Adduct decomposition temperatures were investigated as a function of catalyst structure by using thermal analysis and spectroscopic techniques. Importantly, unlike adducts derived from chloroform, the new pentafluorobenzene-based adducts are more readily prepared and are stable at room temperature. The utility of these adducts as organic catalyst precursors for living ring-opening polymerization (ROP) of lactide, transesterification reactions, and the synthesis of N-heterocyclic carbene ligated organometallic complexes is also described.
