6779-25-5 Usage
Uses
Used in Pharmaceutical Industry:
Urea, N-(diphenylphosphinyl)-N'-phenylis used as a catalyst in the synthesis of pharmaceuticals for its ability to facilitate various organic reactions, which are crucial in the production of complex drug molecules. Its catalytic properties enable the efficient and selective formation of desired compounds, thereby enhancing the overall process of drug development and manufacturing.
Used in Agrochemical Industry:
In the agrochemical sector, Urea, N-(diphenylphosphinyl)-N'-phenylis utilized as a catalyst for the synthesis of agrochemicals, including pesticides and herbicides. Its role in catalyzing key organic reactions allows for the production of effective and targeted agrochemicals, contributing to improved crop protection and yield.
Used in Fine Chemicals Industry:
Urea, N-(diphenylphosphinyl)-N'-phenylis employed as a catalyst in the synthesis of fine chemicals, which are high-purity chemicals used in various applications such as fragrances, dyes, and specialty chemicals. Its ability to catalyze complex organic reactions ensures the production of high-quality fine chemicals with specific properties and applications.
Used in Materials Science:
In the field of materials science, Urea, N-(diphenylphosphinyl)-N'-phenylis used as a catalyst for the synthesis of advanced materials with unique properties. Its catalytic capabilities can contribute to the development of new materials with improved performance in various applications, such as electronics, energy storage, and nanotechnology.
Used in Environmental Remediation:
Urea, N-(diphenylphosphinyl)-N'-phenylhas potential applications in environmental remediation, where it can be used as a catalyst to facilitate chemical reactions that break down pollutants or contaminants. Its ability to catalyze a range of organic reactions can be harnessed to develop processes for the treatment of wastewater, soil remediation, and air pollution control, contributing to a cleaner and more sustainable environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6779-25-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,7 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6779-25:
(6*6)+(5*7)+(4*7)+(3*9)+(2*2)+(1*5)=135
135 % 10 = 5
So 6779-25-5 is a valid CAS Registry Number.
6779-25-5Relevant academic research and scientific papers
Some new compounds with P(E)NHC(O) (E = lone pair, O, S) linkage: Synthesis, spectroscopic, crystal structures, theoretical studies, and antimicrobial evaluation
Gholivand, Khodayar,Dorosti, Niloufar
, p. 1417 - 1425 (2013/10/01)
New phosphinoamides, chalcogenides, and amidophosphates were synthesized and characterized by 1H, 13C, 31P NMR, IR spectroscopy, and elemental analysis. The 13C NMR spectra of two phosphinoamides exhibit obvious differences between their 1 J(P,C) coupling constants (128.3 Hz in one compound vs. 439.2 Hz in another compound). Natural bond orbital analysis was performed to clarify the electronic behavior of the title molecules. The crystal structures of three derivatives were determined by X-ray crystallography. The structure of N-(Diphenylphosphino)-2- pyrazinecarboxamide contains two symmetry-independent forms of the molecule with equal occupancy in the lattice. Density functional theory calculations indicate that two conformers of this compound are identical from an energy point of view. Strong intermolecular N-H···O(P) hydrogen bonds lead to a centrosymmetric dimer in Diphenyl N-(2-pyrazinylcarbonyl)phosphoramidate, whereas N-H···(O)C and N-H···N hydrogen bonds in N-(Diphenylphosphino)-2-pyrazinecarboxamide and N-(Diphenylphosphinothioyl)-2-pyrazinecarboxamide sulfide, respectively, form a one-dimensional polymeric chain in their structures. The in vitro antimicrobial activity of the amidophosphates was evaluated against various microbial strains of Gram positive and Gram negative bacteria and fungi.
