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Terephthalaldehyde diimine, also known as 1,4-benzenediylbis(N-phenylmethanimine), is an organic compound with the chemical formula C20H16N2. It is a white crystalline solid that is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. terephthalaldehyde diimine is synthesized by the condensation of terephthalaldehyde with aniline, resulting in a Schiff base. Terephthalaldehyde diimine is of interest in the field of coordination chemistry due to its potential use as a ligand in the formation of metal complexes. It has been studied for its ability to bind with various metal ions, which can lead to the development of new materials with unique properties, such as in catalysis or as sensors. The compound's structure and reactivity make it a valuable building block in the synthesis of more complex organic molecules and coordination compounds.

7105-00-2

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7105-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7105-00-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,0 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7105-00:
(6*7)+(5*1)+(4*0)+(3*5)+(2*0)+(1*0)=62
62 % 10 = 2
So 7105-00-2 is a valid CAS Registry Number.

7105-00-2Relevant academic research and scientific papers

Biomass chitosan-derived nitrogen-doped carbon modified with iron oxide for the catalytic ammoxidation of aromatic aldehydes to aromatic nitriles

Wang, Wei David,Wang, Fushan,Chang, Youcai,Dong, Zhengping

, (2021)

Nitrogen-doped carbon catalysts have attracted increasing research attention due to several advantages for catalytic application. Herein, cost-effective, renewable biomass chitosan was used to prepare a N-doped carbon modified with iron oxide catalyst (Fe2O3@NC) for nitrile synthesis. The iron oxide nanoparticles were uniformly wrapped in the N-doped carbon matrix to prevent their aggregation and leaching. Fe2O3@NC-800, which was subjected to carbonization at 800 °C, exhibited excellent activity, selectivity, and stability in the catalytic ammoxidation of aromatic aldehydes to aromatic nitriles. This study may provide a new method for the fabrication of an efficient and cost-effective catalyst system for synthesizing nitriles.

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