3300-10-5 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(9H-fluoren-9-yl)is utilized as a key building block in organic synthesis for the creation of various complex molecules. Its unique structure and reactivity facilitate the formation of new chemical entities, contributing to the advancement of chemical research and the development of novel compounds.
Used as a Fluorescent Marker or Dye:
In research and laboratory applications, Ethanone, 1-(9H-fluoren-9-yl)serves as a fluorescent marker or dye. Its optical properties allow for the tracking and visualization of molecules in various experimental setups, aiding in the study of molecular interactions and biological processes.
Used in Pharmaceutical Development:
Ethanone, 1-(9H-fluoren-9-yl)may have potential applications in the pharmaceutical industry. Its distinctive properties could be harnessed in the design and synthesis of new drug candidates, potentially leading to the development of innovative therapeutic agents.
Used in Materials Science:
Ethanone, 1-(9H-fluoren-9-yl)-'s unique characteristics also make it a candidate for use in materials science. It could be incorporated into the development of new materials with specific properties, such as improved fluorescence, stability, or other desirable attributes for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3300-10-5 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, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3300-10:
(6*3)+(5*3)+(4*0)+(3*0)+(2*1)+(1*0)=35
35 % 10 = 5
So 3300-10-5 is a valid CAS Registry Number.
3300-10-5Relevant academic research and scientific papers
Yamazaki, Takahisa,Saito, Shin-ichi,Ohwada, Tomohiko,Shudo, Koichi
, p. 5749 - 5752 (1995)
1,2-dicarbonyl compounds reacted with benzene in the presence of a strong acid, trifluoromethanesulfonic acid, to give gem-diphenylated ketones in high yields.The reaction was accelerated when the acidity of the medium was increased, supporting involvement of O,O-diprotonated 1,2-dicarbonyl species (i.e., 1,2-dihydroxyethylene dications) as the active electrophiles.
