820234-18-2 Usage
Derivative of indole
A heterocyclic aromatic organic compound The compound is based on the structure of indole, which is a heterocyclic (containing both carbon and non-carbon atoms in the ring) aromatic (having a stable, delocalized electron system) organic compound.
Contains a 5-methoxy group and a 2-methoxybenzoyl group attached to the indole ring
The compound has specific functional groups attached to the indole ring, which can affect its chemical properties and reactivity.
Potential applications in the pharmaceutical and organic synthesis industries
The compound can be used as a building block in the synthesis of various pharmaceutical drugs and organic compounds, making it potentially useful in these industries.
May possess biological activity and be of interest for pharmacological research
The compound may have biological effects on living organisms, making it of interest for research into potential medical applications.
Safety information and handling procedures should be followed when working with this chemical compound
As with all chemical compounds, proper safety precautions and handling procedures should be followed to prevent harm to individuals or the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 820234-18-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,0,2,3 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 820234-18:
(8*8)+(7*2)+(6*0)+(5*2)+(4*3)+(3*4)+(2*1)+(1*8)=122
122 % 10 = 2
So 820234-18-2 is a valid CAS Registry Number.
820234-18-2Relevant academic research and scientific papers
Albrecht, Markus,Zhang, Jingyu,Li, Jing,Ward, Jas S.,Truong, Khai-Nghi,Rissanen, Kari
, p. 12160 - 12174 (2020)
A catalytic approach for the preparation of indolines by dearomatizing cyclization is presented. FeCl3 acts as a catalyst to afford tetracyclic 5a,6-dihydro-12H-indolo[2,1-b][1,3]benzoxazin-12-ones in good yields. The cyclization also proceeds with tosylamides forming C-N bonds in 53% yield.
