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3-[2-(4-bromo-phenoxy)-acetylamino]-benzofuran-2-carboxylic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1258206-52-8 Structure
  • Basic information

    1. Product Name: 3-[2-(4-bromo-phenoxy)-acetylamino]-benzofuran-2-carboxylic acid methyl ester
    2. Synonyms:
    3. CAS NO:1258206-52-8
    4. Molecular Formula:
    5. Molecular Weight: 404.217
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1258206-52-8.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-[2-(4-bromo-phenoxy)-acetylamino]-benzofuran-2-carboxylic acid methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-[2-(4-bromo-phenoxy)-acetylamino]-benzofuran-2-carboxylic acid methyl ester(1258206-52-8)
    11. EPA Substance Registry System: 3-[2-(4-bromo-phenoxy)-acetylamino]-benzofuran-2-carboxylic acid methyl ester(1258206-52-8)
  • 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: 1258206-52-8(Hazardous Substances Data)

1258206-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1258206-52-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,8,2,0 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1258206-52:
(9*1)+(8*2)+(7*5)+(6*8)+(5*2)+(4*0)+(3*6)+(2*5)+(1*2)=148
148 % 10 = 8
So 1258206-52-8 is a valid CAS Registry Number.

1258206-52-8Downstream Products

1258206-52-8Relevant articles and documents

Synthesis and biological evaluation of 3-substituted-benzofuran-2- carboxylic esters as a novel class of ischemic cell death inhibitors

Suh, Jeehee,Yi, Kyu Yang,Lee, Yun-Suk,Kim, Eunhee,Yum, Eul Kgun,Yoo, Sung-Eun

scheme or table, p. 6362 - 6365 (2010/12/18)

A series of 3-substituted-benzofuran-2-carboxylic esters was synthesized and evaluated for biological activity as ischemic cell death inhibitors in H9c2 cells and rat primary cardiac myocytes under conditions of oxygen and glucose deprivation. The introduction of a sulfur atom at the three-position substituent of the benzofuran ring markedly improved ischemic cell death inhibitory potency. In particular, 3-[2-(4-nitro-phenylsulfanyl)-acetylamino]-benzofuran-2- carboxylic acid ester (10) (EC50 = 0.532 μM, cell death = 6.18%) and 4-chloro-3-[3-(pyridin-2-ylsulfanyl)-propionylamino]-benzofuran-2-carboxylic ester (18) (EC50 = 0.557 μM, cell death = 7.02%) were shown to be the most potent in this series of benzofuran analogs.

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