58335-01-6 Usage
General Description
(1R,2S)-1,2-diphenyl-1,2-dihydroacenaphthylene-1,2-diol is a chemical compound with two phenyl groups attached to a dihydroacenaphthylene core, and two hydroxyl groups (OH) attached to the dihydroacenaphthylene core. It is a chiral molecule, meaning it has non-superimposable mirror images. (1R,2S)-1,2-diphenyl-1,2-dihydroacenaphthylene-1,2-diol has potential applications in the field of organic chemistry and pharmaceuticals due to its unique structure and functional groups. It could be used as a building block for the synthesis of other complex organic molecules, or 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 various industries.
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 articles and documents
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.
