92736-81-7 Usage
Uses
Used in Chemical Synthesis:
1-(2,4-DICHLORO-PHENYL)-2,2,2-TRIFLUORO-ETHANONE is utilized as an intermediate in the production of various chemicals and pharmaceuticals. Its unique chemical structure makes it a valuable component in the synthesis of a range of compounds for different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1-(2,4-DICHLORO-PHENYL)-2,2,2-TRIFLUORO-ETHANONE serves as a key intermediate for the development of new drugs. Its specific properties allow it to be incorporated into the molecular structures of pharmaceuticals, potentially enhancing their efficacy and therapeutic properties.
Used in Research and Development:
1-(2,4-DICHLORO-PHENYL)-2,2,2-TRIFLUORO-ETHANONE is also employed in research and development settings, where its chemical properties are studied and explored for potential applications in new chemical processes or as a precursor to novel compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 92736-81-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,3 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92736-81:
(7*9)+(6*2)+(5*7)+(4*3)+(3*6)+(2*8)+(1*1)=157
157 % 10 = 7
So 92736-81-7 is a valid CAS Registry Number.
92736-81-7Relevant academic research and scientific papers
Highly efficient synthesis of aryl and heteroaryl trifluoromethyl ketones via o-iodobenzoic acid (IBX)
Cheng, Huicheng,Pei, Yu,Leng, Faqiang,Li, Jingya,Liang, Apeng,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng
, p. 4483 - 4486 (2013/07/26)
A two-step process for the synthesis of aryl and heteroaryl trifluoromethyl ketones from the corresponding aldehydes is described. Trifluoromethyl alcohols were prepared from aryl and heteroaryl aldehydes in excellent yields using catalytic amount of K2CO3. The trifluoromethyl alcohols were then oxidized conveniently and efficiently by o-iodoxybenzoic acid (IBX) under mild conditions to get the desired functionalized aryl and heteroaryl trifluoromethyl ketones.
Antifungal 1-aryl-1-fluoroalkyl-2-(1H-1,2,4-triazol-1-yl)ethanols
-
, (2008/06/13)
Compounds of the general formula STR1 or a pharmaceutically or agriculturally acceptable acid addition salt thereof wherein R is 5-chloro-2-pyridyl, phenyl or phenyl substituted by from one to three substituents, each independently selected from F, Cl, Br
