78016-98-5 Usage
Uses
Used in Chemical Research:
2-Trifluoromethylimidazole-4-carboxylic acid is used as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure and functional groups make it a valuable subject for investigation.
Used in Pharmaceutical Development:
2-Trifluoromethylimidazole-4-carboxylic acid is used as a building block or intermediate in the synthesis of pharmaceutical compounds. Its imidazole core and additional functional groups can be exploited to develop new drugs with specific therapeutic properties.
Used in Material Science:
2-Trifluoromethylimidazole-4-carboxylic acid is used as a component in the development of new materials with tailored properties. Its chemical structure can contribute to the creation of materials with improved stability, reactivity, or other desired characteristics.
Used in Agrochemicals:
2-Trifluoromethylimidazole-4-carboxylic acid is used as an active ingredient or intermediate in the development of agrochemicals, such as pesticides or herbicides. Its unique chemical properties can be harnessed to create effective products for agricultural applications.
Used in Dyes and Pigments:
2-Trifluoromethylimidazole-4-carboxylic acid is used as a colorant or intermediate in the production of dyes and pigments. Its chemical structure can contribute to the development of new colors or improve the properties of existing dyes and pigments.
Check Digit Verification of cas no
The CAS Registry Mumber 78016-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,1 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78016-98:
(7*7)+(6*8)+(5*0)+(4*1)+(3*6)+(2*9)+(1*8)=145
145 % 10 = 5
So 78016-98-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H3F3N2O2/c6-5(7,8)4-9-1-2(10-4)3(11)12/h1H,(H,9,10)(H,11,12)
78016-98-5Relevant academic research and scientific papers
Owen, D.,Plevey, R. G.,Tatlow, J. C.
, p. 179 - 186 (1981)
2-Trifluoromethylimidazole, prepared by the reaction of imidazole-2-carboxylic acid with sulphur tetrafluoride, afforded a silver salt which reacted with organohalides (bromomethane, ethyl bromoacetate, N,N-dimethyl-2-chloroethylamine, and chloroacetonitrile) to give the corresponding N-alkylated derivatives. 2-Trifluoromethylimidazole-4,5-dicarboxylic acid was obtained by oxidation of 2-trifluoromethylbenzimidazole, and on decarboxylation gave only traces of 2-trifluoromethylimidazole; the major product was 2-trifluoromethylimidazole-4-carboxylic acid.The di-acid and sulphur tetrafluoride gave 2,4,5-tris(trifluoromethyl)imidazole.
