845823-11-2 Usage
Uses
Used in Pharmaceutical Industry:
4'-METHOXY-2'-METHYL-2,2,2-TRIFLUOROACETOPHENONE is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs and medications.
Used in Chemical Industry:
In the chemical industry, 4'-METHOXY-2'-METHYL-2,2,2-TRIFLUOROACETOPHENONE is employed as an intermediate for the production of a range of chemical products. Its versatility in chemical reactions allows for its use in creating different types of compounds for various applications.
Used in Research and Development:
4'-METHOXY-2'-METHYL-2,2,2-TRIFLUOROACETOPHENONE is utilized in research and development settings to explore its potential applications and to understand its chemical properties better. This can lead to the discovery of new uses and the development of innovative products.
Used in Specialty Chemicals Production:
4'-METHOXY-2'-METHYL-2,2,2-TRIFLUOROACETOPHENONE is also used in the production of specialty chemicals, where its unique characteristics can be leveraged to create high-value products for specific industries or applications.
Check Digit Verification of cas no
The CAS Registry Mumber 845823-11-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,8,2 and 3 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 845823-11:
(8*8)+(7*4)+(6*5)+(5*8)+(4*2)+(3*3)+(2*1)+(1*1)=182
182 % 10 = 2
So 845823-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H9F3O2/c1-6-5-7(15-2)3-4-8(6)9(14)10(11,12)13/h3-5H,1-2H3
845823-11-2Relevant academic research and scientific papers
Liu, Xue,Liu, Long,Huang, Tianzeng,Zhang, Jingjing,Tang, Zhi,Li, Chunya,Chen, Tieqiao
, p. 4930 - 4934 (2021)
The trifluoromethylation of benzoic acids with TMSCF3 was achieved through nucleophilic substitution with the use of anhydrides as an in situ activating reagent. Under the reaction conditions, a wide range of carboxylic acids including the bioactive ones worked well, thus providing a facile and efficient method for preparing aryl trifluoromethyl ketones from the readily available starting materials.
