116412-84-1 Usage
General Description
4-Chloro-3',4'-dimethoxybenzophenone is a chemical compound with the molecular formula C15H13ClO3. It is a benzophenone derivative with a chloro and two methoxy substituents attached to the benzene ring. 4-Chloro-3',4'-dimethoxybenzophenone is commonly used as a photoinitiator in the production of polymer materials, specifically in UV-curable inks, coatings, and adhesives. It absorbs ultraviolet light and initiates a photochemical reaction that leads to the polymerization of the material. Additionally, it may also have pharmaceutical applications due to its structure and potential biological activities. The chemical properties of 4-Chloro-3',4'-dimethoxybenzophenone make it a versatile and important compound in the fields of materials science and pharmaceutical development.
Check Digit Verification of cas no
The CAS Registry Mumber 116412-84-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,1 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116412-84:
(8*1)+(7*1)+(6*6)+(5*4)+(4*1)+(3*2)+(2*8)+(1*4)=101
101 % 10 = 1
So 116412-84-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H13ClO3/c1-18-13-7-6-11(9-14(13)19-2)15(17)10-4-3-5-12(16)8-10/h3-9H,1-2H3
116412-84-1Relevant articles and documents
Synthesis and biological activity of halophenols as potent antioxidant and cytoprotective agents
Zhao, Wanyi,Feng, Xiue,Ban, Shurong,Lin, Wenhan,Li, Qingshan
scheme or table, p. 4132 - 4134 (2010/08/20)
A series of new bromophenols and chlorophenols were prepared by a practical route. The in vitro antioxidative activity of the halophenols was evaluated by the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging assay, and their cytoprotective activity was also tested on hydrogen peroxide (H2O2)-induced injury in human umbilical vein endothelial cells (HUVEC). All halophenols tested displayed moderate to good DPPH radical-scavenging activity, and two bromophenols, 2,3′-dibromo-4,5,6′-trihydroxydiphenylmethanone (16c) and 2,3-dibromo-4,5-dihydroxydiphenylmethanone (17c) exhibited high protective activity against H2O2-induced injury in HUVEC with EC50 values of 0.4 and 0.8 μM, respectively. The preliminary structure-activity relationships of these compounds were also investigated in order to determine the essential structures required for their bioactivities.