103148-85-2 Usage
Uses
Used in Organic Synthesis:
Triphenylphosphoniumchlorid is used as a reactant in various organic synthesis reactions for the production of phosphoranes and phosphonium salts. Its reactivity and stability make it a valuable component in the synthesis of complex organic molecules.
Used in Catalyst Applications:
In the synthesis of organic compounds, triphenylphosphoniumchlorid serves as a catalyst, enhancing the rate of reactions and improving the overall efficiency of the process. Its catalytic properties are particularly useful in the production of pharmaceuticals and other specialty chemicals.
Used in Oxidation Processes:
Triphenylphosphoniumchlorid is known to be a mild and selective oxidizing agent, which makes it suitable for the oxidation of alcohols to aldehydes and ketones. Its selective nature ensures that the desired products are formed without the formation of unwanted by-products, which is crucial in the synthesis of sensitive compounds.
Used in Antimicrobial Applications:
Triphenylphosphoniumchlorid has shown potential as an antimicrobial agent, with studies suggesting its effectiveness against various strains of bacteria and fungi. This makes it a promising candidate for use in the development of new antimicrobial products, such as disinfectants and preservatives, to combat the growing threat of antibiotic-resistant infections.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, triphenylphosphoniumchlorid is used as a building block for the synthesis of various drug molecules. Its versatility in forming different types of chemical bonds allows for the creation of a wide range of therapeutic agents, including those with potent antimicrobial properties.
Used in Chemical Research:
Triphenylphosphoniumchlorid is also utilized in chemical research as a model compound for studying the properties and reactivity of phosphorus-containing compounds. Its unique structure provides insights into the behavior of phosphorus in various chemical environments, contributing to the broader understanding of phosphorus chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 103148-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,1,4 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103148-85:
(8*1)+(7*0)+(6*3)+(5*1)+(4*4)+(3*8)+(2*8)+(1*5)=92
92 % 10 = 2
So 103148-85-2 is a valid CAS Registry Number.
103148-85-2Relevant academic research and scientific papers
One-pot synthesis of indolo[2,3-c]quinolin-6-ones by sequential photocyclizations of 3-(2-azidophenyl)-N-phenylacrylamides
Li, Zhanshan,Wang, Weixia,Zhang, Xiaotian,Hu, Congcong,Zhang, Wei
, p. 73 - 78 (2013/04/24)
A one-pot synthesis of indolo[2,3-c]quinolin-6(7H)-ones was achieved by sequential photocyclizations of 3-(2-azidophenyl)-N-phenylacrylamides in moderate to high yields. The reactions proceeded via photochemical cyclization of aryl azides to form N-phenylindol-2-carbamides and subsequent 6π-electrocyclic reaction and oxidative aromatization to afford the corresponding indolo[2,3-c]quinolin-6(7H)-ones. Georg Thieme Verlag Stuttgart · New York.
Cycloadditions, 9: Intramolecular Diels-Alder Reaction of Allenecarboxanilides; Incorporation of the Amide Nitrogen Atom in Benzo- and Dibenzo-condensated Five-, Six-, and Seven-membered Rings
Diehl, Klaus,Himbert, Gerhard
, p. 2874 - 2888 (2007/10/02)
The allenecarboxanilides 6a-f, the amide nitrogen atom of which is part of a benzo-condensated five-, six-, or seven-membered ring, are synthesized via phosphorus ylides.Thermolysis of 6 in refluxing xylene induces the intramolecular Diels-Alder reaction only in those cases, where the heterocycle is six- or seven-membered.The allenecarboxamide 6b with the six-membered ring bearing only one benzene nucleus in addition furnishes the quinoline derivatives 9 and 10 as main products, while in the case of the allenecarboxamides 6a,c possessing a five-membered heterocycle no reaction takes place whatever.It is tried to explain this different thermolytic behaviour by taking into consideration the spatial arrangement of the two reacting ?-systems (allene and arene) determined by the structure.
