317319-34-9 Usage
Uses
Used in Scientific Research:
2-Fluoro-4-(trifluoromethyl)thiobenzamide is used as a reagent for the synthesis of more complex chemical substances. Its unique structure and properties make it a valuable component in the development of new compounds and materials in various fields of chemistry and related sciences.
Used in Chemical Synthesis:
2-Fluoro-4-(trifluoromethyl)thiobenzamide is employed as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its presence in these processes can contribute to the creation of novel molecules with potential applications in medicine, agriculture, and industry.
Used in Material Science:
In the field of material science, 2-Fluoro-4-(trifluoromethyl)thiobenzamide is used as a building block for the development of new materials with specific properties. Its incorporation into polymers, for example, can lead to materials with enhanced thermal stability, chemical resistance, or other desirable characteristics.
Used in Analytical Chemistry:
2-Fluoro-4-(trifluoromethyl)thiobenzamide can be used as a reference compound or a standard in analytical chemistry for the calibration of instruments or the development of new analytical methods. Its distinct chemical properties make it a useful tool for researchers in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 317319-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 317319-34:
(8*3)+(7*1)+(6*7)+(5*3)+(4*1)+(3*9)+(2*3)+(1*4)=129
129 % 10 = 9
So 317319-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F4NS/c9-6-3-4(8(10,11)12)1-2-5(6)7(13)14/h1-3H,(H2,13,14)
317319-34-9Relevant academic research and scientific papers
Process development for sodelglitazar: A ppar panagonist
Brown, Andrew D.,Davis, Roman D.,Fitzgerald, Russ N.,Glover, Bobby N.,Harvey, Kim A.,Jones, Lynda A.,Liu, Bing,Patterson, Daniel E.,Sharp, Matthew J.
experimental part, p. 297 - 302 (2010/04/22)
Three efficient syntheses of sodelglitazar (1) have been developed. In particular, the third synthesis avoids the use of zinc and eliminates the resulting heavy metal waste stream as well as the potential genotoxic methanesulfonate in the two earlier syntheses. This process produces sodelglitazar in 74% overall yield from readily available thiophenol (8) and thiazole alcohol (3).
