37619-78-6 Usage
Uses
Used in Analytical Chemistry:
Anthracen-9-aldehyde-N,N-diphenyl-hydrazone is used as a reagent for the spectrophotometric determination of aluminum, allowing for the detection and quantification of aluminum ions through the formation of colored complexes.
Used in Biological Research:
In the study of biological oxidation processes, Anthracen-9-aldehyde-N,N-diphenyl-hydrazone serves as a valuable tool, contributing to the understanding of these complex biochemical reactions.
Used in Microscopy:
As a fluorescent dye, Anthracen-9-aldehyde-N,N-diphenyl-hydrazone enhances the visualization of cellular structures and processes in microscopic examinations, aiding researchers in their studies.
Used in Pharmaceutical Research:
Anthracen-9-aldehyde-N,N-diphenyl-hydrazone is being investigated for its potential anti-cancer properties, with the aim of identifying its effectiveness against various types of cancer.
Used in Antimicrobial Research:
Anthracen-9-aldehyde-N,N-diphenyl-hydrazone is also being explored for its possible antimicrobial properties, which could lead to new treatments for bacterial infections and contribute to the development of novel antimicrobial agents.
Check Digit Verification of cas no
The CAS Registry Mumber 37619-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,1 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 37619-78:
(7*3)+(6*7)+(5*6)+(4*1)+(3*9)+(2*7)+(1*8)=146
146 % 10 = 6
So 37619-78-6 is a valid CAS Registry Number.
37619-78-6Relevant academic research and scientific papers
Preparation method of 9-anthraldehyde-1, 1-diphenylhydrazone
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, (2017/02/24)
The invention relates to a preparation method of 9-anthraldehyde-1, 1-diphenylhydrazone. The preparation method comprises that anthracene, phosphorous oxychloride and N, N-dimethyl formamide are added into a reaction container, the materials undergo a reaction at a temperature of 60-120 DEG C for 6-48h to produce 9-anthraldehyde, N-nitrosodiphenylamine, zinc, acetate acid gracial and an alcohol solvent are added into the reaction container, the mixture undergoes a reaction at a temperature of 0-40 DEG C for 1-9h to produce 1, 1-diphenylhydrazine, 9-anthraldehyde and 1, 1-diphenylhydrazine are added into the reaction container, the mixture undergoes a reaction, the reaction product is cooled and precipitated, and the crystals are filtered and then are recrystallized in benzene so that 9-anthraldehyde-1, 1-diphenylhydrazone is obtained. Through simple recrystallization of the desired compound, a product with purity greater than 99.5% is obtained. The preparation method has the advantages of low raw material cost, mild reaction conditions and high desired product yield. The preparation method provides possibility for use of the hydrazone compound as a semi-conducting material in research on organic electroluminescent devices and organic light conductors.
