25186-99-6 Usage
Description
3,3'-Diiodobenzophenone, a chemical compound with the molecular formula C13H8I2O, is a white crystalline solid belonging to the benzophenones class. It is primarily recognized for its role as a photoinitiator in the synthesis of polymers and plastics, as well as for its function as a light absorber in a variety of organic and inorganic systems. Moreover, 3,3'-Diiodobenzophenone has garnered interest for its potential applications in anti-cancer and antibacterial research. However, due to its potential health risks and environmental implications, careful handling of this compound is essential.
Uses
Used in Polymer and Plastics Industry:
3,3'-Diiodobenzophenone is used as a photoinitiator for the production of polymers and plastics. It facilitates the polymerization process under ultraviolet light, enhancing the efficiency and speed of the reaction, which is crucial for manufacturing high-quality products in this industry.
Used in Organic and Inorganic Systems:
In various organic and inorganic systems, 3,3'-Diiodobenzophenone serves as a light absorber. Its ability to absorb light makes it a valuable component in applications requiring light-sensitive materials, such as in the development of certain types of sensors and optical devices.
Used in Pharmaceutical Research:
3,3'-Diiodobenzophenone is used as a subject of study in pharmaceutical research for its potential anti-cancer properties. 3,3'-Diiodobenzophenone's interaction with biological systems is being investigated to understand its possible role in inhibiting or treating cancer cells.
Used in Antibacterial Applications:
Additionally, 3,3'-Diiodobenzophenone is being explored for its potential antibacterial properties. Research is underway to determine its effectiveness in combating bacterial infections, which could lead to new treatments or preventive measures in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 25186-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,8 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25186-99:
(7*2)+(6*5)+(5*1)+(4*8)+(3*6)+(2*9)+(1*9)=126
126 % 10 = 6
So 25186-99-6 is a valid CAS Registry Number.
25186-99-6Relevant articles and documents
Photoalignment layers for liquid crystals from the di-π-methane rearrangement
Cox, Jason R.,Simpson, Jeffrey H.,Swager, Timothy M.
, p. 640 - 643 (2013)
Photoalignment of nematic liquid crystals is demonstrated using a di-π-methane rearrangement of a designed polymer. The alignment mechanism makes use of the strong coupling of the liquid crystal directors to dibenzobarrelene groups. The large structural c
AZA-PYRIDONE COMPOUNDS AND USES THEREOF
-
, (2016/09/26)
Disclosed herein are aza-pyridone compounds, pharmaceutical compositions that include one or more aza-pyridone compounds, and methods of synthesizing the same. Also disclosed herein are methods of ameliorating and/or treating a disease and/or a condition, including an orthomyxovirus infection, with an aza-pyridone compound. Examples of an orthomyxovirus viral infection include an influenza infection.
Synthesis and characterization of fullerene derivatives with perfluoroalkyl groups
Wang, Xuemei,Guo, Yunlong,Xiao, Yi,Zhang, Lei,Yu, Gui,Liu, Yunqi
supporting information; experimental part, p. 3258 - 3262 (2010/05/02)
Two novel C60 fullerene derivatives containing one or two perfluorooctyl groups were designed and efficiently synthesized. Organic field-effect transistors based on the bisperfluorooctyl compound 1 show high mobility up to 6.7 × 10-2 cm2 V-1 s and high on/off ratio up to 5 × 107, which qualifies compound 1 as promising n-type conductor material. The Royal Society of Chemistry 2009.
