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CAS

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895572-18-6

3-chloro-5-(5-chloro-2-methoxyphenoxy)benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 895572-18-6 Structure

  • Basic information

    1. Product Name: 3-chloro-5-(5-chloro-2-methoxyphenoxy)benzonitrile
    2. Synonyms: 3-chloro-5-(5-chloro-2-methoxyphenoxy)benzonitrile
    3. CAS NO:895572-18-6
    4. Molecular Formula:
    5. Molecular Weight: 294.137
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 895572-18-6.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: 3-chloro-5-(5-chloro-2-methoxyphenoxy)benzonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-chloro-5-(5-chloro-2-methoxyphenoxy)benzonitrile(895572-18-6)
    11. EPA Substance Registry System: 3-chloro-5-(5-chloro-2-methoxyphenoxy)benzonitrile(895572-18-6)

  • 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: 895572-18-6(Hazardous Substances Data)

895572-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 895572-18-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,5,7 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 895572-18:
(8*8)+(7*9)+(6*5)+(5*5)+(4*7)+(3*2)+(2*1)+(1*8)=226
226 % 10 = 6
So 895572-18-6 is a valid CAS Registry Number.

895572-18-6Relevant articles and documents

CATECHOL DIETHERS AS POTENT ANTI-HIV AGENTS

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Page/Page column 53-54, (2013/04/25)

The present invention is directed to novel catechol diether compounds, pharmaceutical compositions therefrom and methods for inhibiting reverse transcriptase and treating HIV infections, especially included drug resistant strains of HIV 1 and 2 and/or sec

Computationally-guided optimization of a docking hit to yield catechol diethers as potent anti-HIV agents

Bollini, Mariela,Domaoal, Robert A.,Thakur, Vinay V.,Gallardo-Macias, Ricardo,Spasov, Krasimir A.,Anderson, Karen S.,Jorgensen, William L.

supporting information; experimental part, p. 8582 - 8591 (2012/02/02)

A 5-μM docking hit has been optimized to an extraordinarily potent (55 pM) non-nucleoside inhibitor of HIV reverse transcriptase. Use of free energy perturbation (FEP) calculations to predict relative free energies of binding aided the optimizations by identifying optimal substitution patterns for phenyl rings and a linker. The most potent resultant catechol diethers feature terminal uracil and cyanovinylphenyl groups. A halogen bond with Pro95 likely contributes to the extreme potency of compound 42. In addition, several examples are provided illustrating failures of attempted grafting of a substructure from a very active compound onto a seemingly related scaffold to improve its activity. (Figure presented)

CHEMICAL COMPOUNDS

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Page/Page column 23, (2008/06/13)

This invention relates to biaryl ether derivatives of formula (I), wherein R1, R3, R4, X, W, Y and m are defined in the description, and to compositions containing them and the uses of such derivatives. The compounds of th

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