220227-53-2 Usage
Uses
Used in Pharmaceutical Industry:
4'-Hydroxy-2'-trifluoromethylacetophenone is used as an intermediate in the synthesis of various pharmaceuticals for its unique chemical properties and reactivity. It plays a crucial role in the development of new drugs and the improvement of existing ones.
Used in Organic Chemistry:
4'-Hydroxy-2'-trifluoromethylacetophenone is used as a building block in organic chemistry for its ability to react with other compounds and form new molecules. It is an essential component in the synthesis of complex organic compounds and contributes to the advancement of organic chemistry research.
Used in Agriculture:
4'-Hydroxy-2'-trifluoromethylacetophenone has potential applications in agriculture, particularly in the development of new agrochemicals and pesticides. Its unique chemical properties and reactivity make it a valuable component in the creation of effective and environmentally friendly agricultural products.
Used in Material Science:
4'-Hydroxy-2'-trifluoromethylacetophenone is used in material science for its potential to contribute to the development of new materials with unique properties. Its reactivity and chemical properties make it a promising candidate for use in the synthesis of advanced materials for various applications, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 220227-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,2 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 220227-53:
(8*2)+(7*2)+(6*0)+(5*2)+(4*2)+(3*7)+(2*5)+(1*3)=82
82 % 10 = 2
So 220227-53-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3O2/c1-5(13)7-3-2-6(14)4-8(7)9(10,11)12/h2-4,14H,1H3
220227-53-2Relevant academic research and scientific papers
PROCESS FOR THE PREPARATION OF 1-[4-NITRO-2-(TRIFLUOROMETHYL)PHENYL]-ALKANONES
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, (2021/08/20)
The present invention relates to a process for the preparation of 1-[4-nitro-2-(trifluoromethyl)- phenyl]-alkanones and substituted phenoxyphenyl ketones.
