3300-03-6 Usage
Uses
Used in Pharmaceutical Production:
Ethanone, 1-(9-methyl-9H-fluoren-9-yl)is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to serve as a building block for the creation of new drug molecules, contributing to the development of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, Ethanone, 1-(9-methyl-9H-fluoren-9-yl)is employed as a reagent in the synthesis of complex organic molecules. Its presence in reactions can lead to the formation of new compounds with potential applications in various industries.
Used in Laboratory Research:
Ethanone, 1-(9-methyl-9H-fluoren-9-yl)is also used in academic and research settings for the investigation of chemical reactions and the study of molecular properties. Its role in these studies aids in the advancement of scientific knowledge and the discovery of new applications.
Used in Material Development:
Due to its distinctive chemical structure, Ethanone, 1-(9-methyl-9H-fluoren-9-yl)has potential applications in the development of new materials. It may be incorporated into the design of advanced materials with specific properties, such as improved stability or enhanced reactivity, for use in various industries.
While Ethanone, 1-(9-methyl-9H-fluoren-9-yl)shows promise in these areas, it is important to note that further research is necessary to fully explore its potential uses and to understand its impact on the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 3300-03-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3300-03:
(6*3)+(5*3)+(4*0)+(3*0)+(2*0)+(1*3)=36
36 % 10 = 6
So 3300-03-6 is a valid CAS Registry Number.
3300-03-6Relevant academic research and scientific papers
A Kinetic Study of the Reactions of Carbonyl Ylides Formed by the Addition of Fluorenylidene to Ketones
Wong, P. C.,Griller, D.,Scaiano, J. C.
, p. 6631 - 6635 (2007/10/02)
Fluorenylidene addds to aliphatic ketones to give carbonyl ylide intermediates.With acetone, for example, laser flash photolysis experiments showed that the rate constant for this reaction was 1 x 107 M-1 s-1 in acetonitrile solvent.The resulting carbonyl ylide had an absorption spectrum with λmax = 640 nm in the absence of quenchers underwent ring closure to the corresponding oxirane.The lifetimes, τy, for the ring closure reaction are described by the equation -log(τy/s) = (13.26 +/- 0.11) - (10.96 +/- 0.12) / θ where θ = 2.3RT kcal mol-1.The spectra of the carbonyl ylides could be quenched with rate constants of circa 107 M-1 s-1 by electron-deficient olefins or oxygen.
