908334-04-3 Usage
Uses
Used in Research Applications:
4-Bromo-1,1-(ethylenedioxo)-indane is used as a research chemical for studying its psychoactive effects and potential as a recreational drug. It provides valuable insights into the understanding of its mechanism of action and potential health effects, contributing to the development of safer and more effective substances.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-Bromo-1,1-(ethylenedioxo)-indane is used as a starting material or intermediate in the synthesis of other compounds with potential therapeutic applications. Its unique chemical structure and properties make it a valuable tool for drug discovery and development.
Used in Toxicological Studies:
4-Bromo-1,1-(ethylenedioxo)-indane is used in toxicological studies to evaluate its safety profile and potential health risks associated with its use. This information is crucial for regulatory bodies to establish appropriate guidelines and restrictions on its use, ensuring the safety of the public.
Used in Forensic Analysis:
In forensic science, 4-Bromo-1,1-(ethylenedioxo)-indane can be used as a marker or indicator in the analysis of samples related to drug abuse or illegal drug trafficking. Its detection in biological or environmental samples can provide valuable information for law enforcement agencies in their investigations.
Check Digit Verification of cas no
The CAS Registry Mumber 908334-04-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,3,3 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 908334-04:
(8*9)+(7*0)+(6*8)+(5*3)+(4*3)+(3*4)+(2*0)+(1*4)=163
163 % 10 = 3
So 908334-04-3 is a valid CAS Registry Number.
908334-04-3Relevant articles and documents
Method for synthesizing ozanimod intermediate 4-cyanoindanone
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Page/Page column 8-13, (2019/10/01)
The invention provides a method for synthesizing an ozanimod intermediate 4-cyanoindanone. The synthesis method has mild reactions and a short route, and the product is convenient to separate and purify. Conventionally available chemical materials are used, a highly toxic reagent cyanide and metal catalysts with high cost are avoided, the safety hazard during storage and use is reduced, and the quality control difficulty of a final product is reduced; and the production cost and the treatment cost of three wastes (waste gas, waste water and industrial residue) are also reduced significantly, and the obtained final product has a high yield and high purity. The method for synthesizing 4-cyanoindanone has small harm to the environment, the requirements of green chemistry are met, and large-scale production can be achieved easily.
Hit-to-lead optimization of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of KDR kinase inhibitors
Dinges, Juergen,Akritopoulou-Zanze, Irini,Arnold, Lee D.,Barlozzari, Teresa,Bousquet, Peter F.,Cunha, George A.,Ericsson, Anna M.,Iwasaki, Nobuhiko,Michaelides, Michael R.,Ogawa, Nobuo,Phelan, Kathleen M.,Rafferty, Paul,Sowin, Thomas J.,Stewart, Kent D.,Tokuyama, Ryukou,Xia, Zhiren,Zhang, Henry Q.
, p. 4371 - 4375 (2007/10/03)
A series of 1,4-dihydroindeno[1,2-c]pyrazoles was prepared and evaluated for their enzymatic inhibition of KDR kinase. Computer modeling studies revealed the importance of attaching a basic side chain in predicting the binding mode of those compounds. Fur