32363-46-5 Usage
Uses
Used in Adhesives and Coatings Industry:
3-CHLORO-3'-METHOXYBENZOPHENONE is used as a photoinitiator for the curing process in the production of adhesives and coatings. Its ability to absorb and dissipate UV radiation allows for efficient and rapid curing, resulting in high-quality products with improved performance and durability.
Used in Polymer Industry:
In the polymer industry, 3-CHLORO-3'-METHOXYBENZOPHENONE is used as a photoinitiator to facilitate the polymerization process. This enables the production of various types of polymers with enhanced properties, such as increased strength, flexibility, and resistance to environmental factors.
Used in Plastics and Inks Manufacturing:
3-CHLORO-3'-METHOXYBENZOPHENONE is utilized in the manufacturing of plastics and inks due to its ability to absorb and dissipate UV radiation. This helps in the production of plastics and inks with improved stability, color retention, and resistance to fading or degradation under sunlight exposure.
Used in Sunscreens and Protective Products:
3-CHLORO-3'-METHOXYBENZOPHENONE is used as an active ingredient in sunscreens and other protective products due to its UV-absorbing properties. It helps in providing broad-spectrum protection against harmful UVA and UVB rays, reducing the risk of skin damage, premature aging, and skin cancer.
Used in Pharmaceutical and Fragrance Synthesis:
3-CHLORO-3'-METHOXYBENZOPHENONE is utilized in the synthesis of various pharmaceuticals and fragrances. Its unique chemical properties make it a valuable intermediate in the production of a wide range of compounds with therapeutic or aromatic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 32363-46-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,6 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32363-46:
(7*3)+(6*2)+(5*3)+(4*6)+(3*3)+(2*4)+(1*6)=95
95 % 10 = 5
So 32363-46-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H11ClO2/c1-17-13-7-3-5-11(9-13)14(16)10-4-2-6-12(15)8-10/h2-9H,1H3
32363-46-5Relevant academic research and scientific papers
Mechanochemical Solvent-Free Suzuki–Miyaura Cross-Coupling of Amides via Highly Chemoselective N?C Cleavage
Ma, Yangmin,Shao, Lei,Szostak, Michal,Wang, Ruihong,Zhang, Jin,Zhang, Pei
supporting information, (2022/01/04)
Although cross-coupling reactions of amides by selective N?C cleavage are one of the most powerful and burgeoning areas in organic synthesis due to the ubiquity of amide bonds, the development of mechanochemical, solid-state methods remains a major challe
Palladium-catalyzed cross-coupling of aroyl chlorides with aryl stannanes in the presence of triethylsilane: Efficient access to aromatic ketones
Higashi, Shoko,Uno, Sota,Ohsuga, Yui,Noumi, Maiko,Saito, Ryota
supporting information, (2020/10/12)
Herein, we report the development of a palladium-catalyzed cross-coupling reaction that focuses on the preparation of aromatic ketones. Aroyl chlorides react quickly at 120 °C with aryl stannanes in the presence of Pd(PPh3)4 and Et3SiH to efficiently give the corresponding ketones without the formation of significant decarbonylated byproducts. In other words, the decarbonylative side reaction is practically suppressed by simply adding Et3SiH to the reaction mixture, which reduces the amount of biaryl impurities in the products.
