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2-Hydroxy-1,2-bis(4-hydroxy-3-methoxyphenyl)ethanone, also known as 2-hydroxy-1,2-bis(3,4-dihydroxy-5-methoxyphenyl)ethanone, is a complex organic compound with the molecular formula C16H14O6. It is a derivative of ethanone, featuring two hydroxyl groups and two methoxy groups attached to the phenyl rings. 2-hydroxy-1,2-bis(4-hydroxy-3-methoxyphenyl)ethanone is known for its antioxidant properties and is a key intermediate in the synthesis of various pharmaceuticals and natural products. It is also a component in the synthesis of certain dyes and pigments. The compound's structure allows it to participate in various chemical reactions, making it a versatile building block in organic chemistry.

5463-23-0

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5463-23-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5463-23-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5463-23:
(6*5)+(5*4)+(4*6)+(3*3)+(2*2)+(1*3)=90
90 % 10 = 0
So 5463-23-0 is a valid CAS Registry Number.

5463-23-0Downstream Products

5463-23-0Relevant academic research and scientific papers

Development of Imidazoline-2-one Derivatives as Potential Antifungal and Anthelminthic Agents: in silico and in vitro Evaluation

Chilamakuru, Naresh Babu,Mallela, Vijaya Jyothi,Peraman, Ramalingam,Shaik, Shakir Basha,Simham, Venu,Singirisetty, Triveni

, p. 423 - 433 (2021/11/24)

Based on appropriate values of synthetic accessibility concerning from ADMET properties and docking scores by docking against proteins 3OZU and 1OJ0, a series of 4,5-diphenyl-1H-imidazol-2-ones (I1?15) were synthesized. The key intermediate, 2-hydroxy-1,2-disubstitutedethanones (E1?15) were prepared by benzoin condensation using 2:1 ratio of aromatic aldehydes and thiamine in the presence of alkali. Further, these cyclized ethanones (E1?15) were treated with urea to yield 4,5-diphenyl-1H-imidazol-2-one derivatives (I1?15) and were characterized by IR,1H NMR, Mass spectra, and CHNO analysis. The synthesized compounds were screened for their anthelmintic potential on Pheretima Posthuma along with standard albendazole, and antifungal activity (minimum inhibitory concentration method) on Candida albicans and Aspergillus niger along with standard miconazole. The results revealed that among all the tested compounds I3, I4, and I7 show considerable synthetic accessibility, docking scores, anthelminthic, and antifungal activity.

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