122030-03-9 Usage
Uses
Used in Pharmaceutical Industry:
Benzene,1-chloro-2,4,5-trifluoro-3-(trifluoromethyl)serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Agrochemical Industry:
Benzene,1-chloro-2,4,5-trifluoro-3-(trifluoromethyl)also plays a significant role as an intermediate in the production of agrochemicals. Its application in this industry aids in the creation of pesticides and other agricultural chemicals that are essential for crop protection and increased yield.
Used in Organic Compounds Synthesis:
Beyond its applications in pharmaceuticals and agrochemicals, Benzene,1-chloro-2,4,5-trifluoro-3-(trifluoromethyl)is utilized as an intermediate in the synthesis of a range of other organic compounds. Its versatility in chemical reactions makes it a valuable component in organic chemistry for creating diverse molecules with potential applications across various industries.
Given the serious health risks associated with exposure to Benzene,1-chloro-2,4,5-trifluoro-3-(trifluoromethyl)-, including respiratory system irritation, skin and eye irritation, central nervous system depression, and the potential for fatal respiratory failure, it is imperative that this chemical is handled with extreme caution. Appropriate protective equipment must be used by individuals working with Benzene,1-chloro-2,4,5-trifluoro-3-(trifluoromethyl)- to ensure safety and minimize the risk of adverse health effects.
Check Digit Verification of cas no
The CAS Registry Mumber 122030-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,0,3 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 122030-03:
(8*1)+(7*2)+(6*2)+(5*0)+(4*3)+(3*0)+(2*0)+(1*3)=49
49 % 10 = 9
So 122030-03-9 is a valid CAS Registry Number.
InChI:InChI=1/C7HClF6/c8-2-1-3(9)6(11)4(5(2)10)7(12,13)14/h1H
122030-03-9Relevant articles and documents
Preparation of organozinc compounds from 3-chloroheptafluorotoluene and zinc: The participation of C-F bonds
Krasnov, Vyacheslav I.,Vinogradov, Andrey S.,Platonov, Vyacheslav E.
, p. 168 - 170 (2006)
Organozinc compounds were obtained from 3-chloroheptafluorotoluene and Zn in DMF; the C-Cl bond is mainly involved in this reaction; the addition of SnCl2 changes the main reaction course in the direction of the participation of the C-F bond (p
Reactions of polyfluorobenzenethiols with polyhalomethanes and their derivatives in an alkaline medium
Bredikhin,Maksimov,Gatilov, Yu. V.,Kireenkov,Platonov
, p. 1551 - 1559 (2015/12/30)
New process direction was found in the reaction of polyfluoroarenethiols with fluorodichloromethane, chloroform, and bromoform in an alkaline medium consisting in the replacement of the thiol group by a hydrogen atom. This process competes with the formation of expected products, dihalomethyl polyfluoro-aryl sulfides and tris(arylsulfanyl)methanes. In reaction of 2,3,5,6-tetrafluorobenzenethiol with dichloro-methane bis(2,3,5,6-tetrafluorophenylsulfanyl)methane was obtained. Reactions of polyfluoroarenethiols with pentafluorobenzyl chloride occur mainly with the substitution of the chlorine atom, with pentafluorobenzal chloride and with pentafluorobenzotrichloride a substitution of a fluorine atom in the para-position takes place.
