797-98-8 Usage
Uses
Used in Pharmaceutical Research:
6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro-1a,6a-diphenylis used as a potential intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with novel mechanisms of action and therapeutic properties.
Used in Material Science Research:
In the field of material science, 6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro-1a,6a-diphenylis utilized for the development of new materials with specific properties. Its versatility in chemical reactions enables the creation of materials with tailored characteristics for various applications, such as advanced polymers, coatings, or sensors.
Used in Organic Synthesis:
6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro-1a,6a-diphenylserves as a valuable building block in organic synthesis, allowing chemists to construct complex molecular structures with diverse functionalities. Its unique properties and reactivity make it a useful component in the synthesis of a wide range of organic compounds, including natural products, pharmaceuticals, and specialty chemicals.
Used in Chemical Reactions:
Due to its dihydro and diphenyl substitution, 6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro-1a,6a-diphenylis employed in various chemical reactions to explore its reactivity and potential applications. Researchers can utilize 6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro-1a,6a-diphenyl- to study reaction mechanisms, develop new synthetic methods, and discover novel chemical transformations.
Used in Academic Research:
6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro-1a,6a-diphenylis a valuable subject of study in academic research, where scientists investigate its properties, reactivity, and potential applications. 6H-Indeno[1,2-b]oxiren-6-one, 1a,6a-dihydro-1a,6a-diphenylcan contribute to the advancement of knowledge in organic chemistry, material science, and related fields, fostering innovation and the development of new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 797-98-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 797-98:
(5*7)+(4*9)+(3*7)+(2*9)+(1*8)=118
118 % 10 = 8
So 797-98-8 is a valid CAS Registry Number.
797-98-8Relevant academic research and scientific papers
Ruf, Sven G.,Bergstr??er, Uwe,Regitz, Manfred
, p. 2219 - 2225 (2000)
Thermolysis of 2,3-diphenylindenone 2,3-epoxide (1) in the presence of tert-butylphosphaalkyne (3) proceeds through a regiospecific 1,3-dipolar cycloaddition of the phosphaalkyne to the carbonyl ylide intermediate to furnish the polycyclic phosphaalkene derivative 4. Compound 4 exhibits a remarkable - and for phosphaalkenes unusual - stability: thus, it can be stored for several days and no decomposition can be observed even in the absence of inert gas protection. The phosphaalkene 4 reacts with 1,3-dipoles such as ethyl diazoacetate (8) by formal transfer of its phosphaalkene unit to afford the 1,2,4-diazaphosphole 10. Addition of lithium alkoxides to the phosphaalkene unit of the polycyclic compound 4 occurs diastereoselectively to give the novel phosphinites 13 and 14. In this context it should be mentioned that the choice of the lithium alkoxide has a decisive influence on the preferred formation of one diastereomer of the phosphinite.
A NEW PHOTO/THERMOCHROMIC SOLID COMPOUND OF THE INDENONE OXIDE FAMILY
Hadjoudis, E.,Pulima, I.
, p. 29 - 36 (2007/10/02)
A new strong photochromic solid compound, a 3-ketone of the 2,3-diphenylindenone oxide, has been prepared for first time.The new compound exhibits very strong photochromic and thermochromic phenomena.
