873092-23-0 Usage
Derivative of isoindole dione
The compound is derived from isoindole dione, which is a chemical structure that consists of a six-membered aromatic ring with two ketone groups (C=O) on adjacent carbon atoms.
Contains a 2-propenyl group
The compound also has a 2-propenyl group, which is a three-carbon chain with a double bond between the first and second carbon atoms, and a hydrogen atom on the second carbon.
Used in organic synthesis and pharmaceutical research
The compound is commonly used in these fields due to its potential biological activities.
Potential as an antitumor and anti-inflammatory agent
The compound has been studied for its ability to inhibit the growth of cancer cells and reduce inflammation.
Ability to inhibit enzymes and protein-protein interactions
The compound has been found to interfere with the activity of certain enzymes and the interactions between proteins, which can be useful in the development of new drugs.
Valuable for further research and development in medicinal chemistry
The compound's structure and properties make it a promising candidate for further study in the development of new therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 873092-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,0,9 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 873092-23:
(8*8)+(7*7)+(6*3)+(5*0)+(4*9)+(3*2)+(2*2)+(1*3)=180
180 % 10 = 0
So 873092-23-0 is a valid CAS Registry Number.
873092-23-0Relevant academic research and scientific papers
Zhang, Lingjuan,Dong, Chaonan,Ding, Chenjun,Chen, Jing,Tang, Weijun,Li, Huanrong,Xu, Lijin,Xiao, Jianliang
, p. 1570 - 1578 (2013)
A general and convenient palladium-catalyzed oxidative Heck arylation of both N-protected and N,N-diprotected allylic amines with arylboronic acids under mild conditions has been developed. The catalyst system, consisting of Pd(OAc)2 (palladium acetate), AgOAc (silver acetate) and KHF 2 (potassium hydrogen fluoride), could efficiently catalyze the coupling reaction in acetone without the aid of any ligand, leading exclusively to the γ-arylated allylic amine products in good to excellent yields. This method is highlighted with excellent regio- and stereocontrol and remarkable functional group tolerance. The carbamate moiety in allylic amine substrates is of crucial importance to the catalytic performance, and the chelation between the carbonyl O (oxygen) and Pd (palladium) atoms is believed to be responsible for the high regioselectivity and stereoselectivity observed. Copyright
