58335-01-6 Usage
Uses
Used in Organic Chemistry:
(1R,2S)-1,2-diphenyl-1,2-dihydroacenaphthylene-1,2-diol is used as a building block for the synthesis of other complex organic molecules. Its unique structure and functional groups make it a valuable component in the creation of new compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
(1R,2S)-1,2-diphenyl-1,2-dihydroacenaphthylene-1,2-diol is used as a starting material for the development of new drugs or biologically active compounds. Its properties and reactivity make it an interesting target for further research and potential applications in the pharmaceutical field, contributing to the discovery of innovative treatments and therapies.
Used in Research and Development:
(1R,2S)-1,2-diphenyl-1,2-dihydroacenaphthylene-1,2-diol is used as a subject of study in research and development initiatives. Its unique structure and functional groups make it an intriguing target for scientists to explore its properties, reactivity, and potential applications in various fields, thereby expanding the knowledge and capabilities of the scientific community.
Check Digit Verification of cas no
The CAS Registry Mumber 58335-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 58335-01:
(7*5)+(6*8)+(5*3)+(4*3)+(3*5)+(2*0)+(1*1)=126
126 % 10 = 6
So 58335-01-6 is a valid CAS Registry Number.
58335-01-6Relevant academic research and scientific papers
C-C Bond Cleavage in O-Centered Mono- and Dianions Derived from α-Dicarbonyl Compounds
Varea, Teresa,Medio, Mercedes,Ballesteros, Rafael,Oniga, Ovidiu,Asensio, Gregorio
, p. 10093 - 10100 (2007/10/02)
The reaction of organolithium compounds with oxalyl derivatives and cyclic 1,2-dicarbonyl compounds leads to pinacols or ketones derived from homolytic C-C bond cleavage of the intermediate O,O-centered pinacol dianions depending on the ability of the substituents for the stabilisation of the resulting radical anion.The homolysis is induced by electrostatic repulsion of the negatively charged oxygen atoms.
