25889-38-7 Usage
Uses
Used in Pharmaceutical Industry:
4-chloro-2-nitro-1-(trifluoromethyl)benzene is used as an intermediate in the synthesis of pharmaceutical compounds due to its chemical reactivity and versatility. The presence of the trifluoromethyl, chlorine, and nitro groups allows for further chemical modifications, making it a valuable building block in the development of new drugs.
Used in Dye Industry:
4-chloro-2-nitro-1-(trifluoromethyl)benzene is used as a starting material for the production of dyes. The unique combination of functional groups in the molecule contributes to the color properties of the resulting dyes, making it a useful component in the creation of various colorants.
Used in Polymer Industry:
4-chloro-2-nitro-1-(trifluoromethyl)benzene is used as a monomer in the synthesis of polymers. The presence of the trifluoromethyl group and other functional groups can influence the polymer's properties, such as its stability, solubility, and reactivity, making it a valuable component in the development of new polymer materials.
Check Digit Verification of cas no
The CAS Registry Mumber 25889-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,8 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 25889-38:
(7*2)+(6*5)+(5*8)+(4*8)+(3*9)+(2*3)+(1*8)=157
157 % 10 = 7
So 25889-38-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClF3NO2/c8-4-1-2-5(7(9,10)11)6(3-4)12(13)14/h1-3H
25889-38-7Relevant academic research and scientific papers
Deoxofluorination of (Hetero)aromatic Acids
Alekseenko, Anatoliy N.,Bugera, Maksym Ya.,Gerus, Igor I.,Kiriakov, Oleksandr,Klipkov, Anton A.,Mykhailiuk, Pavel K.,Pustovit, Yurii,Razhyk, Bohdan,Semenov, Sergey,Starova, Viktoriia S.,Tananaiko, Oksana Yu.,Tarasenko, Karen,Tolmachev, Andrei A.,Trofymchuk, Serhii,Zaporozhets, Olga A.
, p. 3110 - 3124 (2020/03/23)
Diverse trifluoromethyl-substituted compounds were synthesized by deoxofluorination of cinnamic and (hetero)aromatic carboxylic acids with sulfur tetrafluoride. The obtained products were used as starting materials in the preparation of novel fluorinated amino acids, anilines, and aliphatic amines - valuable building blocks for medicinal chemistry and agrochemistry.
