3457-41-8 Usage
Uses
Used in Organic Synthesis:
1,2-di(naphthalen-1-yl)ethane-1,2-dione is used as an intermediate in organic synthesis for its ability to facilitate the creation of complex organic molecules, contributing to the development of various chemical products.
Used in Dye and Pigment Production:
In the dye and pigment industry, 1,2-di(naphthalen-1-yl)ethane-1,2-dione serves as a building block, leveraging its chemical structure to produce a spectrum of dyes and pigments that are utilized in coloring textiles, plastics, and other materials.
Used in Antioxidant and Pharmaceutical Synthesis:
1,2-di(naphthalen-1-yl)ethane-1,2-dione is utilized as a potent oxidizing agent in the synthesis of antioxidants, which are crucial in preventing oxidative damage in various industrial applications. Furthermore, its role extends to the pharmaceutical sector, where it contributes to the development of new drugs.
Used in Anti-Cancer Research:
Although still in the research phase, 1,2-di(naphthalen-1-yl)ethane-1,2-dione has been studied for its potential anti-cancer properties, indicating a possible future application in oncology for the treatment of various cancers.
Safety Considerations:
It is imperative to handle 1,2-di(naphthalen-1-yl)ethane-1,2-dione with care due to its toxic nature. Ingestion, inhalation, or skin absorption can lead to harmful effects, necessitating proper safety measures during its use in any application.
Check Digit Verification of cas no
The CAS Registry Mumber 3457-41-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3457-41:
(6*3)+(5*4)+(4*5)+(3*7)+(2*4)+(1*1)=88
88 % 10 = 8
So 3457-41-8 is a valid CAS Registry Number.
3457-41-8Relevant academic research and scientific papers
The carbonylaiion of organolithium compounds: a polar or a radical mechanism?
Nudelman, Norma Sbarbati,Doctorovich, Fabio,Linares, Guadalupe Garcia,Schulz, Hernaen,Mendiara, Sara
, p. 19 - 24 (2007/10/03)
A variety of riethods were utilized to study the mechanism of carbonylation of organolithium compounds. Convincing evidence that the reaction of aryllithium compounds takes place by radical pathways, being the electron transfer from aryllithium to CO the first rate-determining step, is presented. On the other hand, in the rt actions of lithium dialkylamides no evidence for radical intermediates was found.
Kinetic Study of the Reaction of Naphthyllithium with Carbon Monoxide in Hexane-Tetrahydrofurane Solution
Nudelman, N. Sbarbati,Doctorovich, Fabio
, p. 1233 - 1238 (2007/10/02)
The rate of reaction of naphthyllithium, 1 , with CO in 80:20 hexane-tetrahydrofuran (THF) was studied at 25 deg C.The determined second order kinetic law was found to be first order with respect to 1 and CO.The observed specific rate coeeficient is 6.63 +/- 0.35 dm3 mol-1 s-1.Radical scavengers were observed to inhibit the CO uptake: this result, as well as the kinetic studies, are consistent with an electron transfer as the first and rate-determineng step of the reaction.The rate of the reaction between 1 and THF was also determined and found to be 1E5 times slower than the reaction of 1 with CO.
