569-72-2 Usage
Description
1-(2,2-DIFLUORO-1-PHENYL-VINYL)-4-FLUORO-BENZENE, with the molecular formula C14H8F3, is a synthetic organic compound characterized by a benzene ring with a vinyl group and fluorine atoms at the 2nd and 2nd' positions, along with a fluorine atom at the 4th position. 1-(2,2-DIFLUORO-1-PHENYL-VINYL)-4-FLUORO-BENZENE is known for its unique chemical structure and potential applications in various fields.
Uses
Used in Organic Synthesis:
1-(2,2-DIFLUORO-1-PHENYL-VINYL)-4-FLUORO-BENZENE is used as a building block in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new and effective compounds for different applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(2,2-DIFLUORO-1-PHENYL-VINYL)-4-FLUORO-BENZENE serves as a valuable component for the creation of novel drugs, potentially leading to advancements in the treatment of various diseases and conditions.
Used in Fluorescent Dye Industry:
Due to its unique chemical structure, 1-(2,2-DIFLUORO-1-PHENYL-VINYL)-4-FLUORO-BENZENE has potential applications as a fluorescent dye, which can be utilized in various research and diagnostic applications.
Used in Organic Light-Emitting Diodes (OLEDs):
1-(2,2-DIFLUORO-1-PHENYL-VINYL)-4-FLUORO-BENZENE may also be employed as a material for organic light-emitting diodes (OLEDs), contributing to the development of more efficient and advanced display technologies.
Used in Biological Research:
1-(2,2-DIFLUORO-1-PHENYL-VINYL)-4-FLUORO-BENZENE may possess biological activity, making it a useful research tool for understanding the molecular basis of certain diseases and potentially leading to the discovery of new therapeutic approaches.
Check Digit Verification of cas no
The CAS Registry Mumber 569-72-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 569-72:
(5*5)+(4*6)+(3*9)+(2*7)+(1*2)=92
92 % 10 = 2
So 569-72-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H9F3/c15-12-8-6-11(7-9-12)13(14(16)17)10-4-2-1-3-5-10/h1-9H
569-72-2Relevant articles and documents
Visible-light-promotedE-selective synthesis of α-fluoro-β-arylalkenyl sulfidesviathe deoxygenation/isomerization process
Li, Yuxiu,Li, Xiangqian,Li, Xiaowei,Shi, Dayong
supporting information, p. 2152 - 2155 (2021/03/06)
Regioselective synthesis of α-fluoro-β-arylalkenyl sulfides has been established withgem-difluoroalkenes and sodium sulfinates in a transition-metal-free manner. A series of control experiments were executed to demonstrate thiol radicals and anions as the proposed intermediates. Notably, regioselectiveZ→Eisomerization was achieved under green light irradiation in the absence of a photoinitiator.
From C1 to C3: Copper-Catalyzed gem-Bis(trifluoromethyl)olefination of α-Diazo Esters with TMSCF3
Hu, Jinbo,Hu, Mingyou,Liu, Qinghe,Ni, Chuanfa,Pan, Shitao,Wang, Qian,Xie, Qiqiang
supporting information, p. 8507 - 8511 (2020/04/15)
A Cu-catalyzed gem-bis(trifluoromethyl)olefination of α-diazo esters, using TMSCF3 as the only fluorocarbon source, has been developed and provides an exquisite method to access gem-bis(trifluoromethyl)alkenes. This unprecedented olefination pr
Direct α-Monofluoroalkenylation of Heteroatomic Alkanes via a Combination of Photoredox Catalysis and Hydrogen-Atom-Transfer Catalysis
Tian, Hao,Xia, Qing,Wang, Qiang,Dong, Jianyang,Liu, Yuxiu,Wang, Qingmin
, p. 4585 - 4589 (2019/06/17)
In this study, a new C(sp3)-H monofluoroalkenylation reaction involving cooperative visible-light photoredox catalysis and hydrogen-atom-transfer catalysis to afford products generated by selective hydrogen abstraction and radical-radical cross-coupling was described. This mild, efficient reaction shows high regioselectivity for the α-carbon atoms of amines, ethers, and thioethers and thus allows the preparation of monofluoroalkenes bearing various substituents. The reaction was applied to two bioactive molecules, indicating its utility for late-stage monofluoroalkenylation of compounds with inert C(sp3)-H bonds.
