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CAS

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1415584-43-8

2-phenyl-3-vinylquinoxaline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1415584-43-8 Structure

  • Basic information

    1. Product Name: 2-phenyl-3-vinylquinoxaline
    2. Synonyms:
    3. CAS NO:1415584-43-8
    4. Molecular Formula:
    5. Molecular Weight: 235.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1415584-43-8.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: 2-phenyl-3-vinylquinoxaline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenyl-3-vinylquinoxaline(1415584-43-8)
    11. EPA Substance Registry System: 2-phenyl-3-vinylquinoxaline(1415584-43-8)

  • 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: 1415584-43-8(Hazardous Substances Data)

1415584-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415584-43-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,5,8 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1415584-43:
(9*1)+(8*4)+(7*1)+(6*5)+(5*5)+(4*8)+(3*4)+(2*4)+(1*3)=158
158 % 10 = 8
So 1415584-43-8 is a valid CAS Registry Number.

1415584-43-8Downstream Products

1415584-43-8Relevant articles and documents

Highly efficient vinylaromatics generation via iron-catalyzed sp 3 C-H bond functionalization CDC reaction: A novel approach to preparing substituted benzo[α]phenazines

Lou, Shao-Jie,Xu, Dan-Qian,Shen, Dan-Feng,Wang, Yi-Feng,Liu, Yun-Kui,Xu, Zhen-Yuan

, p. 11993 - 11995 (2012)

An iron-catalyzed benzylic vinylation was developed to transfer the carbon atom in the N,N-dimethyl moiety of N,N-dimethylacetamide (or N,N-dimethylformamide) to 2-methyl azaarenes to generate 2-vinyl azaarenes. The Royal Society of Chemistry.

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