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1-(5-hexyl-2,4-dihydroxyphenyl)-2-(4-nitrophenoxy)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1532534-69-2

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1532534-69-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1532534-69-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,2,5,3 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1532534-69:
(9*1)+(8*5)+(7*3)+(6*2)+(5*5)+(4*3)+(3*4)+(2*6)+(1*9)=152
152 % 10 = 2
So 1532534-69-2 is a valid CAS Registry Number.

1532534-69-2Downstream Products

1532534-69-2Relevant articles and documents

ANTI-VIRULENCE COMPOSITIONS AND METHODS

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Paragraph 00140, (2014/05/07)

A method of reducing the virulence of a bacterium that expresses accessory gene regulator A (AgrA) or an ortholog of AgrA includes administering to the bacterium an amount of a pharmaceutical composition effective to inhibit the synthesis of one or more virulence factors by the bacterium, the pharmaceutical composition including an AgrA antagonist.

Combinatorial synthesis and in vitro evaluation of a biaryl hydroxyketone library as antivirulence agents against mrsa

Yu, Guanping,Kuo, David,Shoham, Menachem,Viswanathan, Rajesh

, p. 85 - 91 (2014/03/21)

Antibiotic resistance coupled with decreased development of new antibiotics necessitates the search for novel antibacterial agents. Antivirulence agents offer an alternative to conventional antibiotics. In this work, we report on a family of small-molecule antivirulence agents against methicillin-resistant Staphylococcus aureus (MRSA), the most widespread bacterial pathogen. Structure-activity relationship studies led to the development of a concise synthesis of a 148-member biarylhydroxyketone library. An acylation bond-forming process afforded resorcinols (1) and aryloxy acetonitriles (2) as synthons. A Lewis-acid-activated Friedel-Crafts' acylation step involving a nitrile functionality of 2 by ZnCl2, followed by nucleophilic attack by 1 was executed to obtain biaryl hydroxyketones in excellent yields. A large number of products crystallized. This strategy affords a range of biarylhydroxyketones in a single step. This is the first collective synthetic study documenting access to this class of compounds through a single synthetic operation. In vitro efficacy of compounds in this library was evaluated by a rabbit erythrocyte hemolysis assay. The most efficacious compound, 4f-12, inhibits hemolysis by 98.1 ± 0.1% compared to control in the absence of the compound.

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