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CAS

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54326-26-0

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

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  • 54326-26-0 Structure

  • Basic information

    1. Product Name: Perfluoropropylbenzene
    2. Synonyms: Perfluoropropylbenzene
    3. CAS NO:54326-26-0
    4. Molecular Formula:
    5. Molecular Weight: 336.08
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 54326-26-0.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: Perfluoropropylbenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: Perfluoropropylbenzene(54326-26-0)
    11. EPA Substance Registry System: Perfluoropropylbenzene(54326-26-0)

  • 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: 54326-26-0(Hazardous Substances Data)

54326-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54326-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,3,2 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 54326-26:
(7*5)+(6*4)+(5*3)+(4*2)+(3*6)+(2*2)+(1*6)=110
110 % 10 = 0
So 54326-26-0 is a valid CAS Registry Number.

54326-26-0Relevant articles and documents

FLUORINATION OF POLYHALOGENATED UNSATURATED COMPOUNDS WITH VANADIUM PENTAFLUORIDE

Bardin, V. V.,Avramenko, A. A.,Furin, G. G.,Krasilnikov, V. A.,Karelin, A. I.,et al.

, p. 385 - 400 (2007/10/02)

Vanadium pentafluoride reacts with polyfluorinated and polychlorinated olefins, alkadienes, cycloalkenes and cyclodienes in CFCl3 or without a solvent at -25 deg C to 100 deg C, forming products of addition of two fluorine atoms across the C=C bond.

REACTION OF POLYHALOGENATED UNSATURATED COMPOUNDS WITH VANADIUM PENTAFLUORIDE

Petrov, V. A.,Bardin, V. V.,Furin, G. G.,Avramenko, A. A.,Galakhov, M. V.,et al.

, p. 37 - 41 (2007/10/02)

Terminal polyhalogenoalkenes are fluorinated by vanadium pentafluoride at -20 to -30 deg C, whereas internal polyfluoroalkenes only react with vanadium pentafluoride when heated. 2-Chloropentafluoro-1,3-butadiene adds fluorine atoms predominantly at positions 1,4 under the influence of vanadium pentafluoride, but only the isomeric tetrafluorohexachlorobutanes are formed from perchloro-1,3-butadiene.Fluorination of perfluoroallylbenzene and perfluoro-β-methylstyrene takes place more rapidly in the side chain than in the aromatic ring.

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