163082-41-5 Usage
Structure
Fluorinated phenanthrene ring attached to an ethanone group
The compound has a complex structure consisting of a modified phenanthrene ring and an ethanone group.
Usage
Organic synthesis and pharmaceutical research
Mainly used in the synthesis of organic compounds and research in pharmaceuticals.
Electron-withdrawing properties
Trifluoromethyl group
The presence of the trifluoromethyl group imparts strong electron-withdrawing properties to the compound.
Applications
Preparation of pharmaceutical intermediates and agrochemicals
Due to its electron-withdrawing nature, it is useful in making various pharmaceutical intermediates and agrochemicals.
Building block
Synthesis of novel materials and new chemical reactions
The compound serves as a building block in creating new materials and developing innovative chemical reactions.
Potential applications
Various fields of chemistry and industry
The unique structure and properties of 2,2,2-trifluoro-1-phenanthren-9-yl-ethanone make it suitable for a wide range of applications in both chemistry and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 163082-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,0,8 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 163082-41:
(8*1)+(7*6)+(6*3)+(5*0)+(4*8)+(3*2)+(2*4)+(1*1)=115
115 % 10 = 5
So 163082-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H9F3O/c17-16(18,19)15(20)14-9-10-5-1-2-6-11(10)12-7-3-4-8-13(12)14/h1-9H
163082-41-5Relevant academic research and scientific papers
Ban, Shu-Rong,Cao, Ya-Fang,Dai, Hui-Xiong,Wang, Xing,Xu, Hui,Yi, Xing
, (2020)
A palladium-catalyzed fluoroacylation of (hetero)aryl boronic acid with the fluorothioacetates is described at ambient temperature. A variety of aryl, and heteroaryl boronic acids are compatible in the reaction, affording the corresponding fluoroalkyl ketones in moderate to good yields. Further late-stage di-, and trifluoroacylation of drug molecule clofibrate and estrone demonstrated the synthetic practicability of this protocol.2009 Elsevier Ltd. All rights reserved.
