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1-(5-ethyl-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.

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  • 618066-20-9 Structure
  • Basic information

    1. Product Name: 1-(5-ethyl-2,4-dihydroxyphenyl)-2-(4-nitrophenoxy)ethanone
    2. Synonyms:
    3. CAS NO:618066-20-9
    4. Molecular Formula:
    5. Molecular Weight: 317.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 618066-20-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(5-ethyl-2,4-dihydroxyphenyl)-2-(4-nitrophenoxy)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(5-ethyl-2,4-dihydroxyphenyl)-2-(4-nitrophenoxy)ethanone(618066-20-9)
    11. EPA Substance Registry System: 1-(5-ethyl-2,4-dihydroxyphenyl)-2-(4-nitrophenoxy)ethanone(618066-20-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 618066-20-9(Hazardous Substances Data)

618066-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 618066-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,1,8,0,6 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 618066-20:
(8*6)+(7*1)+(6*8)+(5*0)+(4*6)+(3*6)+(2*2)+(1*0)=149
149 % 10 = 9
So 618066-20-9 is a valid CAS Registry Number.

618066-20-9Downstream Products

618066-20-9Relevant 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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