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2-Styryl-5-methyl-benzo-furan is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40724-10-5

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  • 40724-10-5 Structure
  • Basic information

    1. Product Name: 2-Styryl-5-methyl-benzo-furan
    2. Synonyms:
    3. CAS NO:40724-10-5
    4. Molecular Formula:
    5. Molecular Weight: 234.298
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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: 2-Styryl-5-methyl-benzo-furan(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Styryl-5-methyl-benzo-furan(40724-10-5)
    11. EPA Substance Registry System: 2-Styryl-5-methyl-benzo-furan(40724-10-5)
  • 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: 40724-10-5(Hazardous Substances Data)

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40724-10-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40724-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,2 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 40724-10:
(7*4)+(6*0)+(5*7)+(4*2)+(3*4)+(2*1)+(1*0)=85
85 % 10 = 5
So 40724-10-5 is a valid CAS Registry Number.

40724-10-5Downstream Products

40724-10-5Relevant academic research and scientific papers

Simple, convenient, and efficient synthesis of 2-aryl-substituted benzo[b]furans

Jiang, Yong,Gao, Botao,Huang, Wenjuan,Liang, Yongmin,Huang, Guosheng,Ma, Yongxiang

experimental part, p. 197 - 204 (2009/04/07)

A simple, convenient, and efficient one-pot method for the preparation of benzofuran is reported. Sonogashira coupling reaction of aryl iodides with 2-methyl-3-butyn-2-ol was used as an acetylene source in the presence of Pd(PPh3)2Cl2 and CuI. Deprotection of the acetylene moiety in the same pot using a strong base and the second Sonogashira coupling/cyclization of and substituted o-iodophenols led to the formation of the appropriate benzo[b]furans. These protocols also can be used in the synthesis of natural products and indoles. Copyright Taylor & Francis Group, LLC.

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