23043-41-6 Usage
Uses
Used in Organic Synthesis:
1-methylacridine is used as a building block in organic synthesis for the creation of various chemical compounds and materials.
Used in Dye Production:
1-methylacridine is used as a precursor in the production of dyes, contributing to the coloration and properties of these products.
Used in Pharmaceutical Industry:
1-methylacridine is used as a starting material or intermediate in the development of pharmaceuticals, potentially leading to new medications.
Used in Agrochemicals:
1-methylacridine is utilized in the formulation of agrochemicals, which are essential for crop protection and enhancement of agricultural yields.
Used as a Fluorescent Tag in Research:
1-methylacridine is used as a fluorescent tag in biological and chemical research, aiding in the visualization and tracking of molecules and cellular processes.
Used in Anti-Cancer Research:
1-methylacridine is investigated for its potential anti-cancer activities, with the aim of developing new therapeutic agents for cancer treatment.
Used in Anti-Microbial Research:
1-methylacridine is explored for its potential anti-microbial properties, which could lead to the development of new antimicrobial agents to combat resistant infections.
Check Digit Verification of cas no
The CAS Registry Mumber 23043-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23043-41:
(7*2)+(6*3)+(5*0)+(4*4)+(3*3)+(2*4)+(1*1)=66
66 % 10 = 6
So 23043-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H11N/c1-10-5-4-8-14-12(10)9-11-6-2-3-7-13(11)15-14/h2-9H,1H3
23043-41-6Relevant academic research and scientific papers
Shen, Jun,Liu, Xi,Wang, Liang,Chen, Qun,He, Mingyang
, p. 1354 - 1362 (2018)
An Rh(III)-catalyzed synthesis of unsymmetrical acridines from aldehydes and azides through bilateral cyclization process in biomass-derived γ-valerolactone has been developed. The in situ-generated imino directing group (DG) from aldehyde and catalytic a
Rh(III)-Catalyzed bilateral cyclization of aldehydes with nitrosos toward unsymmetrical acridines proceeding with C-H functionalization enabled by a transient directing group
Hu, Weiming,Zheng, Qingheng,Sun, Song,Cheng, Jiang
, p. 6263 - 6266 (2017/07/07)
A Rh(iii)-catalyzed bilateral cyclization was developed for the efficient construction of acridines proceeding with C-H functionalization whereby in situ formation and removal of an imino transient directing group in the presence of catalytic amount of BnNH2 are achieved. In this transformation, a sequential Rh(iii)-catalyzed C-H amination, cyclization, and aromatization process was involved.
N-arylation of isatins
-
, (2008/06/13)
A process for the N-arylation of isatins with organo bismuth reagents is disclosed.
