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3,5-bis(2-methoxyphenyl)-1-phenyl-1H-1,2,4-triazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1376268-49-3

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1376268-49-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1376268-49-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,6,2,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1376268-49:
(9*1)+(8*3)+(7*7)+(6*6)+(5*2)+(4*6)+(3*8)+(2*4)+(1*9)=193
193 % 10 = 3
So 1376268-49-3 is a valid CAS Registry Number.

1376268-49-3Downstream Products

1376268-49-3Relevant academic research and scientific papers

Deferasirox (ExJade): An FDA-Approved AIEgen Platform with Unique Photophysical Properties

Sedgwick, Adam C.,Yan, Kai-Cheng,Mangel, Daniel N.,Shang, Ying,Steinbrueck, Axel,Han, Hai-Hao,Brewster, James T.,Hu, Xi-Le,Snelson, Dylan W.,Lynch, Vincent M.,Tian, He,He, Xiao-Peng,Sessler, Jonathan L.

supporting information, p. 1278 - 1283 (2021/02/01)

Deferasirox, ExJade, is an FDA-approved iron chelator used for the treatment of iron overload. In this work, we report several fluorescent deferasirox derivatives that display unique photophysical properties, i.e., aggregation-induced emission (AIE), excited state intramolecular proton transfer, charge transfer, and through-bond and through-space conjugation characteristics in aqueous media. Functionalization of the phenol units on the deferasirox scaffold afforded the fluorescent responsive pro-chelator ExPhos, which enabled the detection of the disease-based biomarker alkaline phosphatase (ALP). The diagnostic potential of these deferasirox derivatives was supported by bacterial biofilm studies.

Copper(II)-catalyzed aerobic oxidative synthesis of substituted 1,2,3- and 1,2,4-triazoles from bisarylhydrazones via C-H functionalization/C-C/N-N/C-N bonds formation

Guru, Murali Mohan,Punniyamurthy, Tharmalingam

, p. 5063 - 5073 (2012/07/16)

An unprecedented copper(II)-catalyzed aerobic oxidative synthesis of 2,4,5-triaryl-1,2,3-triazoles and 1,3,5-triaryl-1,2,4-triazoles from bisarylhydrazones as the common starting precursor has been achieved via cascade C-H functionalization/C-C/N-N/C-N bonds formation under mild reaction conditions. One of the enthralling outcomes of this strategy is the copper(II)-catalyzed room temperature C-H functionalization/C-N bond formation in presence of air, which has been accomplished during the synthesis of substituted 1,2,4-triazoles. This new class of compounds could give prospective luminescence as an iconic component in the area of pharmaceutical and biological sciences. The intermediates for both the processes have been isolated to elucidate the mechanistic scenario.

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