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1453124-78-1

C24H18F12N4O2S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1453124-78-1 Structure

  • Basic information

    1. Product Name: C24H18F12N4O2S2
    2. Synonyms:
    3. CAS NO:1453124-78-1
    4. Molecular Formula:
    5. Molecular Weight: 686.545
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1453124-78-1.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: C24H18F12N4O2S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H18F12N4O2S2(1453124-78-1)
    11. EPA Substance Registry System: C24H18F12N4O2S2(1453124-78-1)

  • 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: 1453124-78-1(Hazardous Substances Data)

1453124-78-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1453124-78-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,3,1,2 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1453124-78:
(9*1)+(8*4)+(7*5)+(6*3)+(5*1)+(4*2)+(3*4)+(2*7)+(1*8)=141
141 % 10 = 1
So 1453124-78-1 is a valid CAS Registry Number.

1453124-78-1Downstream Products

1453124-78-1Relevant articles and documents

Dianhydrohexitols: New tools for organocatalysis. Application in enantioselective Friedel-Crafts alkylation of indoles with nitroalkenes

Chen, Ling-Yan,Guillarme, Stephane,Saluzzo, Christine

, p. 227 - 244 (2013/06/27)

A series of hydrogen bonding organocatalysts was synthesized from dianhydrohexitol and was used for the first time in organocatalysis for Friedel-Crafts alkylation of indoles with nitroalkenes. Moderate yields and enantioselectivities were achieved. ARKAT

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