50562-17-9 Usage
Uses
Used in Chemical Synthesis:
1-(2,2-difluoroethyl)-3-(trifluoromethyl)benzene is used as a building block in the chemical synthesis industry for creating a variety of compounds due to its unique structure and fluorine-containing groups.
Used in Pharmaceutical Processes:
In the pharmaceutical industry, 1-(2,2-difluoroethyl)-3-(trifluoromethyl)benzene is utilized as a starting material for the development of new pharmaceuticals, leveraging its reactive nature and structural properties to form novel drug candidates.
Used in Agrochemical Production:
1-(2,2-difluoroethyl)-3-(trifluoromethyl)benzene also finds application in the agrochemical sector, where it serves as a starting material for the production of new agrochemicals, potentially enhancing the effectiveness of pesticides and other agricultural products.
Caution:
Despite its potential utility, 1-(2,2-difluoroethyl)-3-(trifluoromethyl)benzene should be handled with care due to its highly reactive nature, which may pose health hazards if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 50562-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,6 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 50562-17:
(7*5)+(6*0)+(5*5)+(4*6)+(3*2)+(2*1)+(1*7)=99
99 % 10 = 9
So 50562-17-9 is a valid CAS Registry Number.
50562-17-9Relevant academic research and scientific papers
Copper-Catalyzed Deaminative Difluoromethylation
Cai, Aijie,Liu, Wei,Wang, Yufei,Yan, Wenhao,Yang, Dongqi,Yang, Kundi,Zacate, Samson B.,Zeng, Xiaojun
supporting information, p. 16398 - 16403 (2020/07/17)
The difluoromethyl group (CF2H) is considered to be a lipophilic and metabolically stable bioisostere of an amino (NH2) group. Therefore, methods that can rapidly convert an NH2 group into a CF2H group would be of great value to medicinal chemistry. We report herein an efficient Cu-catalyzed approach for the conversion of alkyl pyridinium salts, which can be readily synthesized from the corresponding alkyl amines, to their alkyl difluoromethane analogues. This method tolerates a broad range of functional groups and can be applied to the late-stage modification of complex amino-containing pharmaceuticals.
