25186-99-6

Usage

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.

Upstream product

• 119-61-9 benzophenone 
• 21222-05-9 3,3'-dinitrobenzophenone 
• 611-79-0 3,3'-diaminobenzophenone 

Downstream Products

• 53304-22-6 Bis-(3-phenylethynyl-phenyl)-methanone 
• 930274-37-6 bis-(3-iodo-phenyl)-methanol 
• 1244029-38-6 C₅₃H₅₈O₉ 
• 1025955-04-7 acetic acid bis-(3-iodo-phenyl)-methyl ester 

Relevant academic research and scientific papers

Photoalignment layers for liquid crystals from the di-π-methane rearrangement

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

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.

Designed synthesis of multi-electrochromic systems bearing diaryl ketone and isophthalates

New multi-electrochromic systems have been developed through the combination of a diaryl ketyl radical system with isophthalate-based electrochromic materials. The location of the isophthalate group in compounds is very critical to obtaining different colors in the multi-electrochromism.

Synthesis and characterization of fullerene derivatives with perfluoroalkyl groups

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.

Superactivity and dual reactivity of the system N-iodosuccinimide-H 2SO4 in the iodination of deactivated arenes

Dissolution of N-iodosuccinimide in sulfuric acid gives rise to electrophilic iodine-containing species which are capable of successfully iodinating aromatic compounds with electron-withdrawing substituents in the temperature range from 0 to 20°C. The iodination in sulfuric acid is effected by both protonated N-iodosuccinimide and IOS(O)(OH+)OH intermediate.

Oxidative iodination of deactivated arenes in concentrated sulfuric acid with I2/NaIO4 and KI/NaIO4 iodinating systems

Deactivated arenes were mono- or diiodinated with strong electrophilic I+ reagents, which were prepared from NaIO4 and either I2 or KI in concentrated H2SO4 (minimum 95% by weight). In general a small excess of the dark brown iodinating solution was used (1.1/1.5 equivalents, for nitrobenzene two equivalents was required). The iodinations were conducted at 25-30 °C with a reaction time of 1-2 hours using either a 'direct' or an 'inverse' method of aromatic iodination to give mono- or diiodinated pure products in 31-91% optimized yields. Georg Thieme Verlag Stuttgart.

Eco-friendly oxidative iodination of various arenes with sodium percarbonate as the oxidant http://www.mdpi.org

Six easy laboratory procedures are presented for the oxidative iodination of various aromatics, mostly arenes, with either molecular iodine or potassium iodide (used as the sources of iodinating species, I+ or I 3+), in the presence of sodium percarbonate (SPC), a stable, cheap, easy to handle, and eco-friendly commercial oxidant.

Eco-friendly Oxidative Iodination of Various Arenes with a Urea-Hydrogen Peroxide Adduct (UHP) as the Oxidant

Three easy eco-friendly laboratory procedures are presented for the oxidative iodination of various activated and deactivated arenes with molecular iodine, in the presence of UHP (percarbamide), a stable, strongly H-bonded, solid urea-hydrogen peroxide adduct as the oxidant.

Chemical Manganese Dioxide (CMD): Its application to the oxidative iodination of benzene, halobenzenes and some deactivated arenes

After comparing our previous and newer results for numerous oxidative aromatic iodination experiments using various brands (of active MnO2 as the oxidants, we recommend the use of a Chemical Manganese Dioxide (Aldrich CMD; 90+% (MnO2) as the oxidant of choice, since it is satisfactorily pure and chemically active, and is notably less costly than other options.