20117-71-9 Usage
Chemical structure
A cyclic compound containing two carbonyl groups (C=O).
Common use
As a reagent in organic synthesis.
Chemical reactions
Can participate in condensation, reduction, and oxidation reactions.
Applications
Potential use in the pharmaceutical and agrochemical industries for the synthesis of active ingredients.
Unique structure
Valuable building block for the production of various organic compounds with diverse functionalities and properties.
Material science
Studied for potential use in materials science.
Fluorescent probe
Investigated for use as a fluorescent probe in biological imaging.
Versatility
Broad potential applications across different fields of science and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 20117-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,1 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20117-71:
(7*2)+(6*0)+(5*1)+(4*1)+(3*7)+(2*7)+(1*1)=59
59 % 10 = 9
So 20117-71-9 is a valid CAS Registry Number.
20117-71-9Relevant academic research and scientific papers
Reactions with Nitrosodisulfonate, 41. Oxidation of Some Enols, Enamines, and Alcohols
Teuber, Hans-Joachim,Hohn, Juergen,Gholami, Abbas
, p. 1309 - 1319 (2007/10/02)
4,6-Dimethyl-1,3-cyclohexanedione is oxidized by potassium nitrosodisulfonate to the vicinal triketone 1. 5-Phenyl- and 5,5-pentamethylene-1,3-cyclohexanedione react with the aldehyde, produced by the dehydrogenation of the alcohol of the solvent, instead with the oxidant to give 2a, b and 3a. 1,2-Indanedione forms the ketol 5a, 1,3-indanedione mainly bindone.The splitting of a carbon-carbon bond is observed in the case of 2-methyl-1,3-cyclohexanedione (-> 5,6-dioxo-n-heptanoic acid), 1,2-cyclohexanedione (-> adipic acid), and dibenzyl ketone (-> benzoic acid). 1,3-Cycloheptanedione does not react.Skatole is oxidized to 2-(formylamino)-5-hydroxyacetophenone, and the Fischer base with ring enlargement to the stereoisomeric quinoline derivatives 12a and b.
