220239-69-0 Usage
Uses
Used in Chemical Synthesis:
2-Fluoro-5-(Trifluoromethyl)Benzyl Bromide is used as a reagent in chemical synthesis for the production of various chemical products. Its reactivity allows it to participate in a range of chemical reactions, contributing to the development of new compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Fluoro-5-(Trifluoromethyl)Benzyl Bromide is used as an intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity make it a valuable component in the creation of new drugs and medicinal agents.
Used in Material Science:
2-Fluoro-5-(Trifluoromethyl)Benzyl Bromide is utilized in material science for the development of advanced materials with specific properties. Its incorporation into polymers and other materials can enhance their characteristics, such as stability, durability, and resistance to environmental factors.
Used in Industrial Processes:
In industrial processes, 2-Fluoro-5-(Trifluoromethyl)Benzyl Bromide is employed as a catalyst or reactant to facilitate specific reactions or improve the efficiency of manufacturing processes. Its use can lead to the production of higher quality products and more sustainable manufacturing methods.
Check Digit Verification of cas no
The CAS Registry Mumber 220239-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,3 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220239-69:
(8*2)+(7*2)+(6*0)+(5*2)+(4*3)+(3*9)+(2*6)+(1*9)=100
100 % 10 = 0
So 220239-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrF4/c9-4-5-3-6(8(11,12)13)1-2-7(5)10/h1-3H,4H2
220239-69-0Relevant academic research and scientific papers
tBuOK-Promoted Cyclization of Imines with Aryl Halides
Li, Ya-Wei,Zheng, Hong-Xing,Yang, Bo,Shan, Xiang-Huan,Qu, Jian-Ping,Kang, Yan-Biao
, p. 4553 - 4556 (2020/06/08)
A transition-metal-free indole synthesis using radical coupling of 2-halotoluenes and imines via the later-stage C-N bond construction was reported for the first time. It includes an aminyl radical generation by C-H cleaving addition of 2-halotoluenes to imines via the carbanion radical relay and an intramolecular coupling of aryl halides with aminyl radicals. One standard condition can be used for all halides including F, Cl, Br, and I. No extra oxidant or transition metal is required.
