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1612222-92-0

C13H12N2O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1612222-92-0 Structure

  • Basic information

    1. Product Name: C13H12N2O2
    2. Synonyms: C13H12N2O2
    3. CAS NO:1612222-92-0
    4. Molecular Formula:
    5. Molecular Weight: 228.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1612222-92-0.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: C13H12N2O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H12N2O2(1612222-92-0)
    11. EPA Substance Registry System: C13H12N2O2(1612222-92-0)

  • 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: 1612222-92-0(Hazardous Substances Data)

1612222-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1612222-92-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,2,2,2 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1612222-92:
(9*1)+(8*6)+(7*1)+(6*2)+(5*2)+(4*2)+(3*2)+(2*9)+(1*2)=120
120 % 10 = 0
So 1612222-92-0 is a valid CAS Registry Number.

1612222-92-0Downstream Products

1612222-92-0Relevant articles and documents

Expedient synthesis of α-(2-azaheteroaryl) acetates via the addition of silyl ketene acetals to azine- N -oxides

Londregan, Allyn T.,Burford, Kristen,Conn, Edward L.,Hesp, Kevin D.

, p. 3336 - 3339 (2014/07/08)

A new and expedient synthesis of α-(2-azaheteroaryl) acetates is presented. The reaction proceeds rapidly under mild conditions via the addition of silyl ketene acetals to azine-N-oxides in the presence of the phosphonium salt PyBroP. This procedure affords diverse α-(2-azaheteroaryl) acetates which are highly desirable components/building blocks in molecules of pharmaceutical interest but are traditionally challenging to synthesize via contemporary methods. The reaction optimization and mechanism as well as a novel electronically enhanced PyBroP derivative are described.

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