18345-95-4 Usage
Uses
Used in Organic Synthesis:
Phenazine, 5-acetyl-5,10-dihydrois used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure and reactivity make it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
Phenazine, 5-acetyl-5,10-dihydrois used as a potential pharmaceutical candidate due to its unique chemical properties. Its ability to interact with biological systems and modulate specific pathways may contribute to the development of new drugs for various therapeutic applications.
Used in Materials Science:
Phenazine, 5-acetyl-5,10-dihydrois used in the development of new materials with specific properties. Its unique structure and reactivity can be exploited to create materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials for energy storage and conversion.
Check Digit Verification of cas no
The CAS Registry Mumber 18345-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,3,4 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18345-95:
(7*1)+(6*8)+(5*3)+(4*4)+(3*5)+(2*9)+(1*5)=124
124 % 10 = 4
So 18345-95-4 is a valid CAS Registry Number.
18345-95-4Relevant academic research and scientific papers
TRICYCLIC HETEROAROMATIC COMPOUNDS AS ALPHA-SYNUCLEIN LIGANDS
-
, (2013/12/04)
Derivatives of phenothiazine, phenoxazine, and phenazine compounds and their use as α-synuclein ligands are described. Also described are methods of using these compounds and their radiolabeled analogs for the detection, monitoring, and treatment of synucleinopathies, including Parkinson's disease.
Photochemical Reductive Acylation and Oxidative Acyl Activation on Phenazine and Related Nitrogen Heterocycles
Takagi, Makoto,Goto, Setsuo,Matsuda, Tsutomu
, p. 1777 - 1778 (2007/10/02)
Irradiation of phenazine in acetaldehyde or propionaldehyde solution gave an N-acylated 5,10-dihydrophenazine.Acridine similarly gave 9-acyl-9,10-dihydroacridine, and 10-methylacridinium salt gave 9-acyl-10-methyl-9,10-dihydroacridine.In methanol N-acylated dihydrophenazines reacted with N-bromosuccinimide to give phenazine and methyl carboxylates in quantitative yield.
