37619-78-6

Basic information

• Product Name: Anthracen-9-aldehyde-N,N-diphenyl-hydrazone
• Synonyms: Anthracen-9-aldehyde-N,N-diphenyl-hydrazone;9-Anthracenecarboxaldehyde 2,2-diphenylhydrazone;9-Anthracenecarboxaldehyde diphenylhydrazone;HY 09;2,2-diphenylhydrazone-9-Anthracenecarboxaldehyde
• CAS NO: 37619-78-6
• Molecular Formula: C27H20N2
• Molecular Weight: 372.4611
• Mol File: 37619-78-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Anthracen-9-aldehyde-N,N-diphenyl-hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Anthracen-9-aldehyde-N,N-diphenyl-hydrazone(37619-78-6)
• EPA Substance Registry System: Anthracen-9-aldehyde-N,N-diphenyl-hydrazone(37619-78-6)

Safety Data

• Hazardous Substances Data: 37619-78-6(Hazardous Substances Data)

Usage

General Description

Anthracen-9-aldehyde-N,N-diphenyl-hydrazone is a chemical compound used in various analytical and biochemical applications. It is a hydrazone derivative of anthracen-9-aldehyde, and it is commonly used as a reagent for the spectrophotometric determination of aluminum. Anthracen-9-aldehyde-N,N-diphenyl-hydrazone forms colored complexes with aluminum ions, allowing for their detection and quantification. Additionally, it has been employed in the study of biological oxidation processes and as a fluorescent dye in microscopy. Anthracen-9-aldehyde-N,N-diphenyl-hydrazone has also been investigated for its potential anti-cancer and antimicrobial properties, making it a versatile and multifunctional chemical compound.

Upstream product

• 120-12-7 anthracene 
• 642-31-9 9-anthracene aldehyde 
• 530-50-7 1,1-Diphenylhydrazine 

Relevant articles and documents

Preparation method of 9-anthraldehyde-1, 1-diphenylhydrazone

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.