122894-73-9 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
Ethyl 2,3,4,5-tetrafluorobenzoate is utilized as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and pesticides. Its unique chemical structure allows for the creation of compounds with specific therapeutic or pesticidal properties.
Used in Insect Repellent Applications:
Due to its strong repellent properties, Ethyl 2,3,4,5-tetrafluorobenzoate is employed as an active ingredient in insect repellent products. It is particularly effective against mosquitoes and other insects, providing protection against bites and the diseases they may transmit.
Used in Chemical Research:
Ethyl 2,3,4,5-tetrafluorobenzoate is also used in chemical research for the study of its properties and potential applications. Its unique structure and reactivity make it a valuable subject for investigations into new chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 122894-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,9 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122894-73:
(8*1)+(7*2)+(6*2)+(5*8)+(4*9)+(3*4)+(2*7)+(1*3)=139
139 % 10 = 9
So 122894-73-9 is a valid CAS Registry Number.
122894-73-9Relevant articles and documents
Regioselective ortho-hydrodefluorination of pentafluorobenzoic acid by low-valent nickel complexes
Adonin,Starichenko
, p. 65 - 67 (2007/10/03)
2,3,4,5-Tetrafluorobenzoic and 3,4,5-trifluorobenzoic acids were prepared in high yields by reaction of C6F5COOH with zinc in the presence of NiCl2-2′-bipyridine (or 1,10-phenanthroline) complexes.
Pyridonecarboxylic acids as antibacterial agents. VIII. Synthesis and structure-activity relationship of 7-(1-aminocyclopropyl)-4-oxo-1,8-naphthyridine-3-carboxylic acids and 7-(1-aminocyclopropyl)-4-oxoquinoline-3-carboxylic acids
Todo,Nitta,Miyajima,Fukuoka,Yamashiro,Nishida,Saikawa,Narita
, p. 2063 - 2070 (2007/10/02)
4-Oxo-1,8-naphthyridine- and 4-oxoquinoline-3-carboxylic acids (2a, b and 3a-l) possessing a 1-aminocyclopropyl group at the 7-position have been synthesized and evaluated for in vitro antibacterial activities. The three quinolones (3d, h, i) exhibited potent antibacterial activities against both gram-positive and gram-negative bacteria, which are comparable to those of ciprofloxacin (CPFX) and ofloxacin (OFLX). Among the three compounds, the best pharmacological and pharmacokinetic profile was obtained with 3i, an OFLX analogue, which was considerably less toxic than three reference quinolones (1, CPFX, and OFLX).
