26902-76-1 Usage
Uses
Used in Chemical Synthesis:
4'-Ethoxyl-2,2,2-trifluoroacetophenone is used as a precursor in the synthesis of various organic compounds. Its unique properties, such as high thermal and chemical stability, make it suitable for use in the production of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4'-Ethoxyl-2,2,2-trifluoroacetophenone is used as a reagent in the synthesis of pharmaceutical compounds. Its strong polar nature and specific chemical activity contribute to the development of new drugs with improved properties and therapeutic effects.
Used in Material Science:
4'-Ethoxyl-2,2,2-trifluoroacetophenone is utilized in material science for the development of new materials with enhanced properties. Its high thermal and chemical stability make it a valuable component in the creation of materials with improved durability and performance.
Used in Laboratory Research:
In laboratory research, 4'-Ethoxyl-2,2,2-trifluoroacetophenone serves as a valuable compound for studying various chemical reactions and processes. Its unique properties allow researchers to explore new reaction pathways and develop innovative synthetic methods.
Overall, 4'-Ethoxyl-2,2,2-trifluoroacetophenone is a versatile chemical compound with a wide range of applications across different industries, including chemical synthesis, pharmaceuticals, material science, and laboratory research. Its unique properties, such as high thermal and chemical stability and strong polar nature, make it an essential component in the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 26902-76-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,0 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26902-76:
(7*2)+(6*6)+(5*9)+(4*0)+(3*2)+(2*7)+(1*6)=121
121 % 10 = 1
So 26902-76-1 is a valid CAS Registry Number.
26902-76-1Relevant academic research and scientific papers
The reduction of aryl trifluoromethyl ketones by sodium borohydride. The hydride transfer process
Stewart, Ross,Teo, K. C.
, p. 2491 - 2496 (2007/10/02)
The rates of reduction of 17 aryl trifluoromethyl ketones by sodium borohydride in 2-propanol have been measured.The rho (ρ) value is 3.12, excluding the 4-amino and 4-dimethylamino groups, which both lower the rate to a greater extent than their ? values predict.The close correspondence between substituent effects for hydride addition in the methyl and trifluoromethyl series (excluding the amino groups) suggests that normal substituent effects are to be expected for oxidation processes involving hydride removal in trifluoromethyl compounds.The present results are consistent with the oxidation of aryl trifluoromethyl carbi ols by permanganate taking place by hydrogen atom abstraction.The effect of substituents on the rate of reduction of the trifluoromethyl ketones is almost identical to that on the equilibrium constant for formation of the ketone hydrates.The application of the reactivity-selectivity principle to the reduction reaction is also considered.Reduction of the 4-ethyl compound has ΔH = 2.7 kcal mol-1 and ΔS = -38 cal deg-1 mol-1.
