886364-44-9 Usage
Uses
Used in Pharmaceutical Industry:
1-(5-Bromo-3-pyridinyl)-2,2,2-trifluoroethanone serves as a key building block in the synthesis of various pharmaceuticals. Its unique combination of trifluoromethyl and bromopyridine groups provides a versatile platform for the development of new drugs with improved pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(5-Bromo-3-pyridinyl)-2,2,2-trifluoroethanone is utilized as a starting material for the creation of novel agrochemicals. Its chemical structure allows for the design of compounds with enhanced pesticidal or herbicidal activities, contributing to more effective crop protection strategies.
Used in Organic Synthesis:
1-(5-Bromo-3-pyridinyl)-2,2,2-trifluoroethanone is employed as an intermediate in organic synthesis, enabling the production of a wide range of chemical compounds. Its reactivity and structural features make it a preferred choice for chemists working on the synthesis of complex organic molecules for various applications.
Used in Research and Development:
1-(5-Bromo-3-pyridinyl)-2,2,2-trifluoroethanone is also used in research and development settings, where its unique properties are explored for potential applications in new materials, catalysts, and other advanced chemical systems. The ability to modify the bromopyridine group further expands the scope of its use in scientific investigations.
Check Digit Verification of cas no
The CAS Registry Mumber 886364-44-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 886364-44:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*4)+(2*4)+(1*4)=219
219 % 10 = 9
So 886364-44-9 is a valid CAS Registry Number.
886364-44-9Relevant 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.
