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CAS

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132257-02-4

Ethanone, 1-(2-amino-4,6-dimethoxyphenyl)-2-chloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132257-02-4 Structure

  • Basic information

    1. Product Name: Ethanone, 1-(2-amino-4,6-dimethoxyphenyl)-2-chloro-
    2. Synonyms: Ethanone, 1-(2-amino-4,6-dimethoxyphenyl)-2-chloro-
    3. CAS NO:132257-02-4
    4. Molecular Formula: C10H12ClNO3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132257-02-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Ethanone, 1-(2-amino-4,6-dimethoxyphenyl)-2-chloro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-(2-amino-4,6-dimethoxyphenyl)-2-chloro-(132257-02-4)
    11. EPA Substance Registry System: Ethanone, 1-(2-amino-4,6-dimethoxyphenyl)-2-chloro-(132257-02-4)

  • 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: 132257-02-4(Hazardous Substances Data)

132257-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132257-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,5 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 132257-02:
(8*1)+(7*3)+(6*2)+(5*2)+(4*5)+(3*7)+(2*0)+(1*2)=94
94 % 10 = 4
So 132257-02-4 is a valid CAS Registry Number.

132257-02-4Relevant articles and documents

2-Arylidenedihydroindole-3-ones: Design, synthesis, and biological activity on bladder carcinoma cell lines

Gerby, Bastien,Boumendjel, Ahcene,Blanc, Madeleine,Bringuier, Pierre Paul,Champelovier, Pierre,Fortune, Antoine,Ronot, Xavier,Boutonnat, Jean

, p. 208 - 213 (2007)

2-Arylidenedihydroindole-3-ones were assayed for their antiproliferative and apoptotic abilities as potential drug candidates to treat bladder tumor. These compounds were tested on cell lines obtained from bladder tumors of various stages [superficial (pT

A short method for the synthesis of 4,6-dimethoxy-1-azaaurones

Lawson, Martin Ata,Mariotte, Anne-Marie,Boumendjel, Ahcene

, p. 149 - 152 (2003)

Aurones (Benzylidenebenzofuran-3(2H)-one) are naturally occurring compounds, which are isomers of the well known flavones. Like flavones, ring A dioxygenated aurones especially on 4 and 6 positions are frequently found in nature and this substitution patt

Synthesis and Biological Activities of 1-Azaaurone Derivatives

Zhang, Min,Li, Ting,Qian, Min,Li, Kailu,Qin, Yukun,Zhao, Ting,Yang, Liu-Qing

, p. 1574 - 1578 (2018)

A series of 1-azaaurone derivatives were designed and synthesized from 3,5-dimethoxyaniline and 2-chloroacetonitrile. Their structures were characterized by melting point, 1H NMR, IR, and elemental analysis, as well as 13C NMR. The t

Substituted aurone derivatives

-

, (2008/06/13)

A method for treating a fungal infection is disclosed. The method includes administering to a patient a pharmaceutical composition containing a compound of formula (IA): where each R is independently H, OH, Br, Cl, I, amino, thiol, nitro, C1-4a

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