25199-86-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-3-(trifluoromethyl)quinoline is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications. Its unique structure and reactivity allow for the creation of compounds with enhanced properties and effectiveness.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-3-(trifluoromethyl)quinoline is utilized as an intermediate in the synthesis of agrochemicals, specifically for the development of pesticides and other crop protection agents. Its antimicrobial and antifungal properties make it a promising candidate for improving agricultural yields and combating plant diseases.
Used in Organic Synthesis:
2-Chloro-3-(trifluoromethyl)quinoline is employed as a valuable building block in organic synthesis, where it is used to construct more complex organic molecules with specific functions and properties. Its versatility in forming various chemical bonds and its compatibility with different reaction conditions make it an essential component in the synthesis of a wide range of organic compounds.
Used in Research and Development:
2-CHLORO-3-(TRIFLUOROMETHYL)QUINOLINE is also used in research and development for the exploration of new materials and drug candidates. Its unique chemical structure and reactivity provide a foundation for the design and synthesis of novel compounds with potential applications in various fields, including medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 25199-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,9 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25199-86:
(7*2)+(6*5)+(5*1)+(4*9)+(3*9)+(2*8)+(1*6)=134
134 % 10 = 4
So 25199-86-4 is a valid CAS Registry Number.
InChI:InChI=1S/C10H5ClF3N/c11-9-7(10(12,13)14)5-6-3-1-2-4-8(6)15-9/h1-5H
25199-86-4Relevant academic research and scientific papers
Recommendable routes to trifluoromethyl-substituted pyridine- and quinolinecarboxylic acids
Cottet, Fabrice,Marull, Marc,Lefebvre, Olivier,Schlosser, Manfred
, p. 1559 - 1568 (2007/10/03)
As part of a case study, rational strategies for the preparation of all ten 2-, 3-, or 4-pyridinecarboxylic acids and all nine 2-, 3-, 4-, or 8-quinolinecarboxylic acids bearing trifluoromethyl substituents at the 2-, 3-, or 4-position were elaborated. The trifluoromethyl group, if not already present in the precursor, was introduced either by the deoxygenative fluorination of suitable carboxylic acids with sulfur tetrafluoride or by the displacement of ring-bound bromine or iodine by trifluoromethylcopper generated in situ. The carboxy function was produced by treatment of organolithium or organomagnesium intermediates, products of halogen/metal or hydrogen/ metal permutation, with carbon dioxide. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).
