3834-66-0 Usage
Description
4-Fluorobenzil, also known as 1-(4-Fluorophenyl)-2-phenylethane-1,2-dione, is an organic compound derived from diphenylacetylene. It is characterized by the presence of a fluorine atom attached to a benzene ring, which distinguishes it from its non-fluorinated counterparts. This structural feature endows 4-Fluorobenzil with unique chemical and physical properties, making it a versatile compound for various applications.
Uses
Used in Pharmaceutical Industry:
4-Fluorobenzil is used as an intermediate compound for the synthesis of benzil derivatives. Its unique fluorinated structure allows for the development of new pharmaceutical compounds with improved properties, such as enhanced bioavailability, increased stability, and better target specificity.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-Fluorobenzil serves as a key building block for the creation of more complex molecules. Its fluorinated nature can be exploited to introduce fluorine-containing moieties into various organic compounds, which may result in improved chemical and biological properties.
Used in Material Science:
4-Fluorobenzil can be utilized in the development of novel materials with specific properties. For instance, its incorporation into polymers or other materials may lead to enhanced thermal stability, increased resistance to degradation, or improved mechanical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 3834-66-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,3 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3834-66:
(6*3)+(5*8)+(4*3)+(3*4)+(2*6)+(1*6)=100
100 % 10 = 0
So 3834-66-0 is a valid CAS Registry Number.
3834-66-0Relevant articles and documents
Electrochemical oxidation-induced benzyl C–H carbonylation for the synthesis of aromatic α-diketones
Tan, Yu-Fang,Chen, Yuan,Li, Rui-Xue,Guan, Zhi,He, Yan-Hong
, (2021/12/21)
Electrochemical oxidation-induced direct carbonylation of benzyl C–H bond for the synthesis of aromatic α-diketones is described. In this process, tetrabutylammonium iodide (nBu4NI) not only acts as an electrolyte, but its iodine anion is oxidized to an iodine radical at the anode, acting as a hydrogen atom transfer agent. The iodine radical extracts the benzyl hydrogen atom and causes the carbonylation of the benzyl position, where O2 in the air is used as an oxygen source.
Visible-Light-Induced Photocatalytic Oxidative Decarboxylation of Cinnamic Acids to 1,2-Diketones
Chand, Shiv,Pandey, Anand Kumar,Singh, Rahul,Singh, Krishna Nand
, p. 6486 - 6493 (2021/05/06)
A concerted metallophotoredox catalysis has been realized for the efficient decarboxylative functionalization of α,β-unsaturated carboxylic acids with aryl iodides in the presence of perylene bisimide dye to afford 1,2-diketones.
Ruthenium/dendrimer complex immobilized on silica-functionalized magnetite nanoparticles catalyzed oxidation of stilbenes to benzil derivatives at room temperature
Ghanaatzadeh, Niloofar,Hashemi, Hajar,Moghadam, Majid,Niknam, Khodabakhsh,Saberi, Dariush
, (2020/02/13)
A new ruthenium/dendrimer complex stabilized on the surface of silica-functionalized nano-magnetite was fabricated and well characterized. The nano-catalyst showed good activity in the synthesis of benzil derivatives via the oxidation of stilbenes with high turnover frequency (TOF) at room temperature. Moreover, the catalyst could also be reused up to fifteen times without any loss of its activity.
