6602-40-0 Usage
Uses
Used in Organic Chemistry:
[2,3'-Bipyrrolidin]-2'-one, 1,1'-diphenylis used as a building block for the synthesis of more complex molecules and pharmaceuticals. Its unique structure allows for the creation of a wide range of compounds with diverse properties and potential applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [2,3'-Bipyrrolidin]-2'-one, 1,1'-diphenylmay have potential biological activities that could be of interest for further research and development. Its unique structure could lead to the discovery of new drugs or therapeutic agents.
Used in Materials Science:
[2,3'-Bipyrrolidin]-2'-one, 1,1'-diphenylhas the potential to exhibit interesting optical and electronic properties, making it a valuable compound for research and development in materials science. Its unique structure could contribute to the creation of new materials with enhanced properties for various applications.
Used in Electronics Applications:
Due to its potential optical and electronic properties, [2,3'-Bipyrrolidin]-2'-one, 1,1'-diphenylmay also find use in the electronics industry. Its unique structure could be harnessed to develop new components or devices with improved performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 6602-40-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6602-40:
(6*6)+(5*6)+(4*0)+(3*2)+(2*4)+(1*0)=80
80 % 10 = 0
So 6602-40-0 is a valid CAS Registry Number.
6602-40-0Relevant academic research and scientific papers
The extraordinary reactions of phenyldimethylsilyllithium with N,N-disubstituted amides
Buswell, Marina,Fleming, Ian,Ghosh, Usha,Mack, Stephen,Russell, Matthew,Clark, Barry P.
, p. 3006 - 3017 (2007/10/03)
The reactions of the silyllithium reagent with tertiary amides was discussed. The enediamines were easily isomerized from cis to trans, easily oxidized to dienediamines and were hydrolyzed to α-aminoketones. If the two equivalents of the silyllithium reagent were used, the product was an α-silylamine. The results show that each member of the homologous series of amides gives rise to a substantially different product.
Thereaction of phenyldimethylsilyllithium with N-phenylpyrrolidone
Buswell, Marina,Fleming, Ian
, p. 202 - 203 (2007/10/03)
Phenyldimethylsilyllithium reacts with N-phenylpyrrolidone 5 to give the known tetracyclic amines [2,3,3a,3b,4,5,6,11b-octahydro-3aα,3bα,11bα-1-phenyl-1H- dipyrrolo(1,2a:3′,2′c)quinoline and its 3bβ isomer] 6 and 7.
