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2-ethyl-5-methoxycyclohexa-2,5-diene-1,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55157-48-7

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55157-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55157-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,1,5 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 55157-48:
(7*5)+(6*5)+(5*1)+(4*5)+(3*7)+(2*4)+(1*8)=127
127 % 10 = 7
So 55157-48-7 is a valid CAS Registry Number.

55157-48-7Downstream Products

55157-48-7Relevant academic research and scientific papers

Primulin derivative as well as synthesis method and application of primulin derivative

-

, (2018/01/11)

The invention discloses a primulin derivative with antibacterial activity shown as the structural general formula (I), wherein R is selected from C2-C20 alkyls. The primulin derivative is prepared from raw materials including m-dihydroxybenzene and a fatty acid derivative by the steps: carrying out Friedel-Crafts acylation and methylation to synthesize a paeonol derivative, and carrying out oxidization after carrying out carbonyl reduction. The primulin derivative has good antibacterial activity and can be used as a potential antibacterial agent.

Synthesis and highly potent hypolipidemic activity of alpha-asarone- and fibrate-based 2-acyl and 2-alkyl phenols as HMG-CoA reductase inhibitors

Mendieta, Aarn,Jimnez, Fabiola,Garduo-Siciliano, Leticia,Mojica-Villegas, Anglica,Rosales-Acosta, Blanca,Villa-Tanaca, Lourdes,Chamorro-Cevallos, Germn,Medina-Franco, Jos L.,Meurice, Nathalie,Gutirrez, Rsuini U.,Montiel, Luisa E.,Cruz, Mara Del Carmen,Tamariz, Joaqun

, p. 5871 - 5882 (2015/01/08)

In the search for new potential hypolipidemic agents, the present study focused on the synthesis of 2-acyl phenols (6a-c and 7a-c) and their saturated side-chain alkyl phenols (4a-c and 5a-c), and on the evaluation of their hypolipidemic activity using a

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