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CAS

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1402228-08-3

5-(4-nitrophenyl)-2-{1-(pyrimidin-2-yl)-1H-indol-2-yl}oxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1402228-08-3 Structure

  • Basic information

    1. Product Name: 5-(4-nitrophenyl)-2-{1-(pyrimidin-2-yl)-1H-indol-2-yl}oxazole
    2. Synonyms: 5-(4-nitrophenyl)-2-{1-(pyrimidin-2-yl)-1H-indol-2-yl}oxazole
    3. CAS NO:1402228-08-3
    4. Molecular Formula:
    5. Molecular Weight: 383.366
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1402228-08-3.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: 5-(4-nitrophenyl)-2-{1-(pyrimidin-2-yl)-1H-indol-2-yl}oxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-(4-nitrophenyl)-2-{1-(pyrimidin-2-yl)-1H-indol-2-yl}oxazole(1402228-08-3)
    11. EPA Substance Registry System: 5-(4-nitrophenyl)-2-{1-(pyrimidin-2-yl)-1H-indol-2-yl}oxazole(1402228-08-3)

  • 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: 1402228-08-3(Hazardous Substances Data)

1402228-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402228-08-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,2,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1402228-08:
(9*1)+(8*4)+(7*0)+(6*2)+(5*2)+(4*2)+(3*8)+(2*0)+(1*8)=103
103 % 10 = 3
So 1402228-08-3 is a valid CAS Registry Number.

1402228-08-3Downstream Products

1402228-08-3Relevant articles and documents

Copper-mediated and copper-catalyzed cross-coupling of indoles and 1,3-azoles: Double C-H activation

Nishino, Mayuko,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro

, p. 6993 - 6997 (2012/10/07)

A new bronze age: The described copper-mediated cross-coupling with double C-H activation can provide a convergent access to indole-containing biheteroaryls that are of high interest in pharmaceutical and medicinal chemistry. In this strategy an easily attachable and detachable 2-pyrimidyl directing group is used. Moreover, a variant that is catalytic in copper is achieved by using atmospheric oxygen as an ideal co-oxidant (see scheme). Copyright

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