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1572248-02-2

2,5-Bis(4-fluorophenyl)-3,6-dimethylpyrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1572248-02-2 Structure

  • Basic information

    1. Product Name: 2,5-Bis(4-fluorophenyl)-3,6-dimethylpyrazine
    2. Synonyms: 2,5-Bis(4-fluorophenyl)-3,6-dimethylpyrazine
    3. CAS NO:1572248-02-2
    4. Molecular Formula:
    5. Molecular Weight: 296.319
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1572248-02-2.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: 2,5-Bis(4-fluorophenyl)-3,6-dimethylpyrazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,5-Bis(4-fluorophenyl)-3,6-dimethylpyrazine(1572248-02-2)
    11. EPA Substance Registry System: 2,5-Bis(4-fluorophenyl)-3,6-dimethylpyrazine(1572248-02-2)

  • 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: 1572248-02-2(Hazardous Substances Data)

1572248-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1572248-02-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,2,2,4 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1572248-02:
(9*1)+(8*5)+(7*7)+(6*2)+(5*2)+(4*4)+(3*8)+(2*0)+(1*2)=162
162 % 10 = 2
So 1572248-02-2 is a valid CAS Registry Number.

1572248-02-2Downstream Products

1572248-02-2Relevant articles and documents

Nitroepoxides as versatile precursors to 1,4-diamino heterocycles

Vidal-Albalat, Andreu,Rodriguez, Santiago,Gonzalez, Florenci V.

, p. 1752 - 1755 (2014)

Nitroepoxides are easily transformed into 1,4-diamino heterocycles such as quinoxalines and pyrazines by treatment with 1,2-benzenediamines and ammonia, respectively. Additionally, related saturated heterocycles, such as piperazines and tetrahydroquinoxalines, can be accessed by treatment with 1,2-diamines and a reducing agent. These transformations are efficient, provide access privileged, bioactive structures, and produce minimal waste.

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