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ethyl 2-triphenylphosphoimino-3-(2-benzofuryl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145161-79-1

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  • 145161-79-1 Structure
  • Basic information

    1. Product Name: ethyl 2-triphenylphosphoimino-3-(2-benzofuryl)acrylate
    2. Synonyms:
    3. CAS NO:145161-79-1
    4. Molecular Formula:
    5. Molecular Weight: 491.526
    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: ethyl 2-triphenylphosphoimino-3-(2-benzofuryl)acrylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-triphenylphosphoimino-3-(2-benzofuryl)acrylate(145161-79-1)
    11. EPA Substance Registry System: ethyl 2-triphenylphosphoimino-3-(2-benzofuryl)acrylate(145161-79-1)
  • 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: 145161-79-1(Hazardous Substances Data)

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145161-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145161-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,6 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 145161-79:
(8*1)+(7*4)+(6*5)+(5*1)+(4*6)+(3*1)+(2*7)+(1*9)=121
121 % 10 = 1
So 145161-79-1 is a valid CAS Registry Number.

145161-79-1Relevant academic research and scientific papers

Condensed O-, N-Heterocycles by the Transformation of Azidoacrylates

Krutosikowa, Alzbeta,Dandarova, Miloslava,Chylova, Jana,Vegh, Daniel

, p. 807 - 816 (2007/10/02)

A number of furopyridines (4a-4d) and benzoderivative (4e), as well as pyrrolofuropyridine (8) were prepared by reaction of the corresponding iminophosphoranes, available from ethyl azidoheteroacrylates and triphenylphosphinee,

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