479499-02-0 Usage
Uses
Used in Organic Synthesis:
2-(E)-Benzylidene-6-(trifluoroacetyl)cyclohexanone is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-(E)-Benzylidene-6-(trifluoroacetyl)cyclohexanone is utilized as an intermediate in the development of new drugs and pharmaceutical compounds, leveraging its unique structural features to enhance drug properties and efficacy.
Used in the Development of Novel Organic Materials:
The trifluoroacetyl group in 2-(E)-Benzylidene-6-(trifluoroacetyl)cyclohexanone is used to impart distinctive properties to molecules, making it instrumental in the creation of innovative organic materials with potential applications in various industries.
Used in Scientific and Industrial Fields:
Due to its structural significance, 2-(E)-Benzylidene-6-(trifluoroacetyl)cyclohexanone is employed across a range of scientific and industrial fields for further study and potential application, including but not limited to chemical engineering, material science, and pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 479499-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,4,9 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 479499-02:
(8*4)+(7*7)+(6*9)+(5*4)+(4*9)+(3*9)+(2*0)+(1*2)=220
220 % 10 = 0
So 479499-02-0 is a valid CAS Registry Number.
479499-02-0Relevant articles and documents
Condensation of 2-polyfluoroacycloalkanones with aldehydes and dimethylformamide-dimethylacetal
Sevenard,Khomutov,Kodess,Pashkevich,Loop,Lork,Roeschenthaler
, p. 157 - 163 (2007/10/03)
Polyfluorinated 1,3-diketones containing carbocycles react with aldehydes under Lewis-acid catalysis and also with dimethylformamide-dimetylacetal without catalysis, yielding exclusively (E)-configured condensation products involving the methylene group of the carbocycle. Novel trifluoromethylated chromenes are prepared from 2-trifluoroacetylcycloalkanones and salicylaldehyde. The structures of two new compounds, 2-(E)-benzylidene-6-trifluoroacetylcyclohexanone and 4-trifluoroacetyl-2,3-dihydro-1H-xantene, are confirmed by X-ray structure analysis.
