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72323-99-0

1,2,3,4-Tetrafluorbenzoldisulfonsaeure is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 72323-99-0 Structure

  • Basic information

    1. Product Name: 1,2,3,4-Tetrafluorbenzoldisulfonsaeure
    2. Synonyms: 1,2,3,4-Tetrafluorbenzoldisulfonsaeure
    3. CAS NO:72323-99-0
    4. Molecular Formula:
    5. Molecular Weight: 310.204
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 72323-99-0.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: 1,2,3,4-Tetrafluorbenzoldisulfonsaeure(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2,3,4-Tetrafluorbenzoldisulfonsaeure(72323-99-0)
    11. EPA Substance Registry System: 1,2,3,4-Tetrafluorbenzoldisulfonsaeure(72323-99-0)

  • 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: 72323-99-0(Hazardous Substances Data)

72323-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72323-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,2 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 72323-99:
(7*7)+(6*2)+(5*3)+(4*2)+(3*3)+(2*9)+(1*9)=120
120 % 10 = 0
So 72323-99-0 is a valid CAS Registry Number.

72323-99-0Upstream product

72323-99-0Downstream Products

72323-99-0Relevant articles and documents

Trimethylsilylesters of Fluorobenzenesulfonic acids

Johannsen, Heiner,Sartori, Peter

, p. 674 - 679 (2007/10/02)

Fluorobenzenesulfonic acids were prepared by electrophilic sulfonation of fluorobenzenes 1.The acids are obtained as hydrates and converted to their trimethylsilyl esters 2 for characterization.

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