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3,3'-(2-hydroxyl-5-nitrophenyl)methylenebisindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

692769-54-3

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692769-54-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 692769-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,2,7,6 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 692769-54:
(8*6)+(7*9)+(6*2)+(5*7)+(4*6)+(3*9)+(2*5)+(1*4)=223
223 % 10 = 3
So 692769-54-3 is a valid CAS Registry Number.

692769-54-3Downstream Products

692769-54-3Relevant academic research and scientific papers

Room-temperature synthesis of diindolylmethanes using silica-supported sulfuric acid as a reusable catalyst under solvent-free conditions

Zhang, Yan,Chen, Xiang,Liang, Jun,Shang, Zhi-Cai

, p. 2446 - 2454 (2011)

Efficient electrophilic substitution reactions of indoles with various aromatic and aliphatic aldehydes were carried out using a catalytic amount of H2SO4SiO2 under solvent-free conditions to afford the corresponding bis(indolyl)methanes in excellent yields.

Chickpea leaf exudates: A green Br?nsted acid type biosurfactant for bis(indole)methane and bis(pyrazolyl)methane synthesis

Patil, Rupesh C.,Damate, Shashikant A.,Zambare, Dnyandev N.,Patil, Suresh S.

supporting information, p. 9152 - 9162 (2021/06/02)

A clean and highly efficient protocol for green synthesis of bis(indole)methanes and bis(pyrazolyl)methanes has been successfully achieved by using a naturally sourced bio-surfactant, chickpea leaf exudates (CLE), as a Br?nsted acid-type catalyst. The rea

A novel approach to bis(indolyl)methanes using nickel nanoparticles as a reusable catalyst under solvent-free conditions

Olyaei, Abolfazl,Vaziri, Mohsen,Razeghi, Reza,Shams, Bahareh,Bagheri, Hasan

, p. 463 - 468 (2013/08/26)

Nano-sized nickel as a catalyst has been developed for the electrophilic substitution reactions of indole with various aromatic aldehydes under solvent-free conditions to afford the corresponding bis(indolyl)methanes in high to excellent yields. The descr

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